Risedronate
Risedronate is a bisphosphonate (a bone-strengthening medicine) used to treat and prevent osteoporosis, including glucocorticoid-induced osteoporosis, to treat osteoporosis in men, and to treat Paget's disease of bone, depending on the product.
🧬 Where this information comes from Click to expand
The clinical label records used on this page are FDA-filed Structured Product Labeling (SPL) retrieved through openFDA. We identified 9 clinical label sets within the page’s selected clinical scope after exact ingredient or ingredient-combination matching and applicable route/form matching. Forms, routes, brands, labelers, strengths, and NDC product-record counts are built separately from matching FDA National Drug Code Directory records. The linked DailyMed document is a representative official source for verification, not the page’s only clinical source. View the linked label on DailyMed →
Risedronate is a bisphosphonate that attaches to bone and slows the cells that break it down, used to treat or prevent osteoporosis and to treat Paget's disease of bone; it is a common first choice for osteoporosis, on the market since the late 1990s and available as a generic. Most people tolerate it well; indigestion, belly upset and back, joint or muscle aches are typical. The main risk is irritation of the esophagus (the swallowing tube), so follow the water and stay-upright rules exactly, and stop it and call your doctor for painful swallowing, chest pain or new heartburn. New thigh or groin pain deserves a prompt call too.
Clinical pearls
- Regular tablets go before any food or drink; Atelvia, the delayed-release form, goes right after breakfast, so check your label.
- Keep up your calcium and vitamin D, but take calcium, antacids, magnesium and iron at a different time of day.
- If you take Atelvia, avoid acid reducers such as omeprazole or famotidine, which can change how the delayed-release tablet is released.
- Tell your dentist before extractions or implants, and tell imaging staff before a bone scan, since risedronate can affect both.
Patient information guide A plain-language walkthrough of Risedronate, written from its FDA label.
What Risedronate is used for
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Risedronate is a bisphosphonate used for several bone conditions, depending on the product.
- Treatment and prevention of postmenopausal osteoporosis (risedronate sodium tablets)
- Treatment of postmenopausal osteoporosis (risedronate sodium delayed-release tablets, including Atelvia)
- Treatment to increase bone mass in men with osteoporosis (risedronate sodium tablets)
- Treatment and prevention of glucocorticoid-induced osteoporosis in men and women starting or continuing long-term steroid treatment (risedronate sodium tablets)
- Treatment of Paget's disease of bone in men and women (risedronate sodium tablets)
How Risedronate works
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Risedronate sticks to bone mineral and slows osteoclasts, the cells that break bone down. This reduces bone turnover and bone loss.
In steroid-related osteoporosis, it lowers bone breakdown without directly blocking bone formation.
Risedronate dosage
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Risedronate is taken by mouth. The tablet types are taken differently, so follow the instructions for your product.
- Risedronate sodium tablets: taken on an empty stomach, at least 30 minutes before the first food, drink or medicine, with 6 to 8 ounces of plain water. Schedules range from daily to monthly depending on the condition.
- Delayed-release tablets: taken once a week in the morning right after breakfast with at least 4 ounces of plain water.
- Stay upright for 30 minutes and swallow whole.
- Missed weekly dose: take one tablet the morning after you remember, then return to your usual day. Never take two tablets on the same day. Missed-dose rules for monthly schedules differ, so ask your pharmacist.
Dosing details from the FDA-approved label
From the Risedronate prescribing information (“Dosage and Administration”). Doses are set by your prescriber for your product, condition, kidney function and age — never change a dose on your own.
- Treatment of Postmenopausal Osteoporosis (film-coated tablet)
- One 5 mg tablet orally, taken daily
- Or one 35 mg tablet orally, taken once-a-week
- Or one 75 mg tablet orally, taken on two consecutive days for a total of two tablets each month
- Or one 150 mg tablet orally, taken once-a-month
- Swallow whole with 6 to 8 ounces of plain water at least 30 minutes before the first food, beverage, or medication of the day; avoid lying down for 30 minutes
- Prevention of Postmenopausal Osteoporosis
- One 5 mg tablet orally, taken daily
- Or one 35 mg tablet orally, taken once-a-week
- Alternatively, one 75 mg tablet orally, taken on two consecutive days for a total of two tablets each month may be considered
- Or alternatively, one 150 mg tablet orally, taken once-a-month may be considered
- Take at least 30 minutes before the first food or drink of the day other than water
- Treatment to Increase Bone Mass in Men with Osteoporosis
- One 35 mg tablet orally, taken once-a-week
- Take at least 30 minutes before the first food or drink of the day other than water
- Treatment and Prevention of Glucocorticoid-Induced Osteoporosis
- One 5 mg tablet orally, taken daily
- Take at least 30 minutes before the first food or drink of the day other than water
- Treatment of Paget's Disease
- 30 mg orally once daily for 2 months
- Retreatment may be considered (following post-treatment observation of at least 2 months) if relapse occurs, or if treatment fails to normalize serum alkaline phosphatase
- Dose and duration for retreatment are the same as for initial treatment
- No data are available on more than 1 course of retreatment
- Treatment of Postmenopausal Osteoporosis (delayed-release tablet)
- One 35 mg delayed-release tablet orally, taken once-a-week
- Take in the morning immediately following breakfast with at least 4 ounces of plain water, not under fasting conditions; avoid lying down for 30 minutes; do not chew, cut, or crush
Read the label’s full dosing text
2 DOSAGE AND ADMINISTRATION Treatment of Postmenopausal Osteoporosis: 5 mg daily, 35 mg once-a-week, 75 mg two consecutive days each month, 150 mg once-a-month ( 2.1 ) Prevention of Postmenopausal Osteoporosis: 5 mg daily, 35 mg once-a-week ( 2.2 ) Men with Osteoporosis: 35 mg once-a-week ( 2.3 ) Glucocorticoid-Induced Osteoporosis: 5 mg daily ( 2.4 ) Paget's Disease: 30 mg daily for 2 months ( 2.5 ) Instruct patients to: • Swallow tablet whole with 6 to 8 ounces of plain water, at least 30 minutes before the first food, beverage, or medication of the day. • Avoid lying down for 30 minutes ( 2 ) • Take supplemental calcium and vitamin D if dietary intake is inadequate ( 2.7 ) 2.1 Treatment of Postmenopausal Osteoporosis [see Indications and Usage (1.1)] The recommended regimen is: • one 5 mg tablet orally, taken daily or • one 35 mg tablet orally, taken once-a-week or • one 75 mg tablet orally, taken on two consecutive days for a total of two tablets each month or • one 150 mg tablet orally, taken once-a-month 2.2 Prevention of Postmenopausal Osteoporosis [see Indications and Usage (1.1)] The recommended regimen is: • one 5 mg tablet orally, taken daily or • one 35 mg tablet orally, taken once-a-week or • alternatively, one 75 mg tablet orally, taken on two consecutive days for a total of two tablets each month may be considered or • alternatively, one 150 mg tablet orally, taken once-a-month may be considered 2.3 Treatment to Increase Bone Mass in Men with Osteoporosis [see Indications and Usage (1.2)] The recommended regimen is: • one 35 mg tablet orally, taken once-a-week 2.4 Treatment and Prevention of Glucocorticoid-Induced Osteoporosis [see Indications and Usage (1.3)] The recommended regimen is: • one 5 mg tablet orally, taken daily 2.5 Treatment of Paget's Disease [see Indications and Usage (1.4)] The recommended treatment regimen is 30 mg orally once daily for 2 months. Retreatment may be considered (following post-treatment observation of at least 2 months) if relapse occurs, or if treatment fails to normalize serum alkaline phosphatase. For retreatment, the dose and duration of therapy are the same as for initial treatment. No data are available on more than 1 course of retreatment.
Excerpted — the section continues on the label. Read the full Dosage and Administration section on DailyMed →
Risedronate side effects
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In studies, the most common side effects were:
Common side effects
- Back pain
- Joint pain (arthralgia)
- Abdominal (belly) pain
- Indigestion (dyspepsia)
- Diarrhea
- Muscle pain
- Nausea
- Constipation
When to get medical help
- Trouble or pain when swallowing, chest pain behind the breastbone, or new or worsening heartburn: stop the medicine and get medical help.
- New thigh or groin pain: this could signal an unusual femur (thigh bone) fracture, so see your doctor.
- Severe bone, joint or muscle pain: tell your doctor, who may stop the medicine.
- Jaw pain, or slow healing after dental work: this could be osteonecrosis of the jaw (damage to jaw bone).
- Signs of low calcium (hypocalcemia): tell your doctor right away.
- Swelling of the face or throat, a widespread rash, or blistering or peeling skin: get urgent help.
- Eye inflammation (iritis, uveitis): rare, but report it.
Call your doctor promptly for painful swallowing, chest pain, new heartburn, severe bone, joint or muscle pain, new thigh or groin pain, jaw problems, or allergic reactions like facial swelling or blistering skin.
Risedronate warnings and precautions
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- Esophagus and stomach irritation: can be severe, especially if you lie down after a dose, skip the full glass of water, or keep taking it despite symptoms.
- Low calcium: must be corrected before starting. Get enough calcium and vitamin D.
- Jaw osteonecrosis: linked to dental procedures, poor oral hygiene and some other therapies; the risk may rise with longer use.
- Severe bone, joint or muscle pain: can start within a day or after several months.
- Unusual thigh fractures: thigh or groin pain may be an early warning.
- Kidneys: not recommended in severe kidney impairment.
- Do not take both delayed-release and regular risedronate tablets.
- Needed treatment length should be rechecked regularly.
Risedronate interactions
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Several common products reduce how much risedronate your body absorbs.
- Calcium supplements and antacids: lower absorption, so separate them.
- Magnesium supplements or laxatives, and iron: also interfere with absorption.
- PPIs and H2 blockers: can speed release of delayed-release tablets; not recommended together.
- Aspirin and NSAIDs: upper stomach and gut side effects occurred in some users.
- Food and other drinks: other than plain water, they can interfere with the regular tablets.
- Estrogen therapy: use together has not been studied.
Interactions listed in the FDA-approved label
From the Risedronate prescribing information (“Drug Interactions”): what the manufacturer studied or reported to the FDA.
- Calcium supplements/antacids: Co-administration of a tablet containing 600 mg of elemental calcium and 400 international units vitamin D reduced risedronate bioavailability by approximately 38% when risedronate was given following breakfast. Should not be taken together; take at a different time of the day.
- Magnesium-based supplements or laxatives: Interfere with the absorption of risedronate sodium. Should not be taken together; take at a different time of the day.
- Iron preparations: Interfere with the absorption of risedronate sodium. Should not be taken together; take at a different time of the day.
- Proton pump inhibitors (PPIs): Drugs that raise stomach pH may cause faster drug release from delayed-release products; esomeprazole increased Cmax by 60 percent and AUC by 22 percent. Concomitant administration is not recommended.
- Histamine 2 (H2) blockers: Drugs that raise stomach pH may cause faster drug release from enteric coated (delayed-release) products such as risedronate sodium. Concomitant administration is not recommended.
- Hormone therapy (estrogens and estrogen agonist/antagonists): Concomitant use with risedronate sodium has not been studied.
- Aspirin/Nonsteroidal Anti-Inflammatory Drugs: In the Phase 3 study, 18% of NSAID users in both groups developed upper gastrointestinal adverse reactions; among non-users, 13% on 35 mg once-a-week and 12% on 5 mg daily did.
- Hepatic microsomal drug-metabolizing enzymes (for example, Cytochrome P450): Risedronate is not metabolized and does not induce or inhibit these enzymes.
Read the label’s full interactions text
7 DRUG INTERACTIONS Risedronate is not metabolized and does not induce or inhibit hepatic microsomal drug-metabolizing enzymes (for example, Cytochrome P450). Calcium supplements, antacids, proton pump inhibitors (PPIs), H 2 blockers, magnesium-based supplements or laxatives, and iron preparations interfere with the absorption of risedronate sodium (7.1, 7.2) 7.1 Calcium Supplements/Antacids When risedronate sodium was administered following breakfast, the co-administration of a tablet containing 600 mg of elemental calcium and 400 international units vitamin D reduced risedronate bioavailability by approximately 38% [ see Clinical Pharmacology (12.3) ]. Calcium supplements, antacids, magnesium-based supplements or laxatives, and iron preparations interfere with the absorption of risedronate sodium and should not be taken together. 7.2 Histamine 2 (H 2 ) Blockers and Proton Pump Inhibitors (PPIs) Drugs that raise stomach pH (for example, PPIs or H 2 blockers) may cause faster drug release from enteric coated (delayed-release) drug products such as risedronate sodium. Co-administration of risedronate sodium with the PPI, esomeprazole, increased risedronate bioavailability. The maximum plasma concentration (C max ) and the area under the plasma concentration (AUC) were increased by 60 percent and 22 percent, respectively. Concomitant administration of risedronate sodium and H 2 blockers or PPIs is not recommended. 7.3 Hormone Therapy Concomitant use of risedronate sodium with estrogens and estrogen agonist/antagonists has not been studied. 7.4 Aspirin/Nonsteroidal Anti-Inflammatory Drugs In the Phase 3 study comparing risedronate sodium 35 mg once-a-week immediately following breakfast and risedronate sodium 5 mg daily, 18% of NSAID users (any use) in both groups developed upper gastrointestinal adverse reactions.
Excerpted — the section continues on the label. Read the full Drug Interactions section on DailyMed →
Not a complete list. The label covers the interactions the manufacturer studied or reported, and our own interaction database does not cover every medicine either. Bring your full medication list, including vitamins and herbal products, to your pharmacist.
Before taking Risedronate
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- Do not take it with esophagus narrowing or slow emptying, low blood calcium, an inability to stay upright for 30 minutes, or allergy to risedronate.
- Tell your doctor about heartburn, swallowing trouble, ulcers, gastritis or Barrett's esophagus.
- Not recommended in severe kidney impairment.
- Pregnancy: stop when pregnancy is recognized. Breastfeeding: your doctor will weigh benefits and risks.
- Not indicated for children.
- Older adults: no overall differences in safety or effectiveness were seen, though greater sensitivity in some cannot be ruled out.
- Liver problems: not studied, but dose changes are unlikely to be needed.
- Before steroid-related osteoporosis treatment, sex hormone status should be checked.
Risedronate overdose
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A large overdose can lower blood calcium and phosphorus and may cause symptoms of low calcium. Seek emergency care or call Poison Control. Treatment may include removing unabsorbed drug from the stomach and giving calcium.
What Risedronate does in the body
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Risedronate lowers the high bone turnover seen in postmenopausal osteoporosis. Bone breakdown markers fall within about 14 days, and bone turnover is lowest by about 6 months, staying stable for up to 3 years. In Paget's disease, bone turnover returned to normal in most people treated for 2 months.
How your body processes Risedronate
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Very little risedronate is absorbed by mouth, and food reduces absorption of regular tablets. About 60% of absorbed drug goes to bone in animal studies. It is not metabolized, and the rest leaves through the urine; unabsorbed drug leaves in stool. Kidney impairment slows clearance.
How to store Risedronate
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Store at 20° to 25°C (68° to 77°F); excursions permitted between 15° and 30°C (59° and 86°F) . Dispense in well-closed containers as defined in USP.
Written from the FDA-approved label with AI and reviewed by our pharmacy team. How we use AI →
Supplements & herbs that interact with Risedronate
23 supplements and herbal products have documented interactions with Risedronate in the licensed clinical database we use. Most are manageable — but your pharmacist should know about everything you take, including vitamins and herbals.
- Major · 1
- Moderate · 13
- Minor · 9
Educational information from a licensed clinical database (Natural Medicines) — see our data sources & update cadence. Not medical advice: an interaction being documented does not mean it will happen to you; do not start or stop medications or supplements without professional guidance.
Risedronate: pharmacist answers to common questions
Quick, plain-English answers to the questions patients ask most about Risedronate — the kind of thing our pharmacy team would talk through with you at the counter.
What is risedronate for?
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How do I take it correctly?
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What side effects should I expect?
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Can I take my calcium or antacid with it?
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What if I miss a weekly dose?
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Is it safe in pregnancy?
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Is Risedronate available over the counter?
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When was Risedronate first available?
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Who makes Risedronate?
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Answers drafted from the FDA-approved label with AI and reviewed by our pharmacy team. How we use AI →
More about Risedronate on HelloPharmacist
Risedronate forms and strengths (how it comes)
Risedronate is available in 2 forms. Different forms and brands can have different approved uses, doses, schedules, and directions. Follow the instructions for your exact product, and do not switch forms without guidance from your prescriber or pharmacist.
Need a version that does not list lactose, a gluten source, a dye or gelatin? Inactive ingredients differ by manufacturer: see Risedronate inactive ingredients by manufacturer.
Tablet
How this form is used
- Risedronate sodium tablets treat and prevent postmenopausal osteoporosis.
- Risedronate sodium tablets treat osteoporosis in men and treat and prevent glucocorticoid-induced osteoporosis.
- Risedronate sodium tablets treat Paget's disease of bone in men and women.
- Take risedronate sodium tablets at least 30 minutes before the first food, drink or medicine of the day.
- Swallow whole with 6 to 8 ounces of plain water and avoid lying down for 30 minutes.
- Do not chew or suck risedronate sodium tablets.
- Schedules vary by condition (daily, weekly, twice monthly or monthly), so follow your prescriber's directions.
Delayed-release tablet
How this form is used
- Risedronate sodium delayed-release tablets are used to treat postmenopausal osteoporosis.
- Risedronate sodium delayed-release tablets are taken once a week in the morning right after breakfast.
- Swallow whole upright with at least 4 ounces of plain water; do not chew, cut or crush.
- Stay upright for 30 minutes after taking risedronate sodium delayed-release tablets.
- If a weekly dose is missed, take one tablet the morning after remembering; never take two on the same day.
Risedronate on the U.S. market: products, makers and brands
How Risedronate appears in the FDA’s National Drug Code Directory — including its dosage forms, strengths, brand names, manufacturers, and FDA-listed product records. These are directory records, not sales or prescription volume.
8 companies list 21 Risedronate product records with the FDA, mostly as tablet, delayed-release tablet; the earliest marketing or approval year on record is 1998. Brand names on the directory include Actonel, Atelvia; the rest are generics.
FDA-listed product records by dose form (tablet variants merged) — FDA National Drug Code Directory. Record counts are not sales or prescription volume.
Also listed with the FDA, not a patient dose form: Powder (9) — bulk drug substance sold to compounders/manufacturers and multi-item kits. These aren’t counted in the dose-form total above.
Share of FDA-listed product records by manufacturer — FDA National Drug Code Directory. Record counts are not sales or prescription volume.
How widely Risedronate is used (Medicaid data)
A general measure of how commonly Risedronate is prescribed, based on Medicaid — one of the largest public drug programs. The figure below is prescriptions filled in Q1–Q4 2025, summed across every form and brand of the drug.
Think of this as a proxy for how widely Risedronate is used, drawn from freely available public data. Medicaid is just one program — these numbers don’t include Medicare, other government coverage, or commercial and cash-pay prescriptions, so real-world use is higher than what’s shown here.
How commonly is Risedronate prescribed? Of the 1,601 medications we measure, Risedronate ranks #1,107 by Medicaid prescriptions — more than 31% of them.
Utilization by Risedronate product
Pick a product to see its own Medicaid numbers. Each chip is one clinical product — a specific strength & dosage form as defined by RxNorm — with brand-name and generic versions combined.
risedronate sodium 150 MG Oral Tablet Most dispensed
Summed across the 7 of 16 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 905028
risedronate sodium 35 MG Oral Tablet
Summed across the 1 of 5 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 905024
risedronate sodium 5 MG Oral Tablet
Summed across the 1 of 15 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 905041
Other Risedronate products — combination packs and listings not yet matched to a specific clinical product (kept visible so every prescription is accounted for)
Summed across the 5 of 34 listed NDC products with Medicaid activity.
Shares are of the Medicaid prescriptions shown here. Product grouping follows RxNorm (the National Library of Medicine’s drug terminology), so “one product” means one strength & dosage form regardless of manufacturer. Dollar figures are gross Medicaid reimbursement before mandatory rebates — rebates (often large, especially for brand-name drugs) are confidential, so actual net cost to Medicaid is lower than shown.
Source: Medicaid State Drug Utilization Data (CMS), aggregated by generic ingredient — summed across every NDC (all brands, strengths, salt forms and dosage forms) of Risedronate, and across all states and both fee-for-service and managed-care claims. A general popularity signal; it excludes Medicare, commercial insurance and cash prescriptions, so it is not total U.S. use. Based on the 14 of 70 listed Risedronate NDCs with Medicaid activity.
Compare Risedronate products
A representative set of FDA-listed product records for Risedronate — across manufacturers, strengths, and dosage forms, grouped by form with each product’s manufacturer and how the FDA approved it. The same medicine may be made and packaged by different companies, so a single drug can have many directory entries. (It’s also why a refill can look different — a new shape, color, or box — even though it contains the same medication.)
| Strength | Route | Manufacturer / Labeler | Category ⓘ | Details |
|---|---|---|---|---|
| 💊Delayed-release tablet | ||||
| 35 mg | Oral | Sun Pharmaceutical Industires Inc. | ANDA | View NDC → |
| 💊Tablet | ||||
| 35 mg | Oral | Apotex Corp. | ANDA | View NDC → |
| 75 mg | Oral | Apotex Corp. | ANDA | View NDC → |
| 150 mg | Oral | Apotex Corp. | ANDA | View NDC → |
| 5 mg | Oral | Aurobindo Pharma Limited | ANDA | View NDC → |
| 30 mg | Oral | Aurobindo Pharma Limited | ANDA | View NDC → |
| 35 mg | Oral | Aurobindo Pharma Limited | ANDA | View NDC → |
| 150 mg | Oral | Aurobindo Pharma Limited | ANDA | View NDC → |
| 35 mg | Oral | Hangzhou Minsheng Binjiang Pharmaceutical CO., Ltd | ANDA | View NDC → |
| 5 mg | Oral | Macleods Pharmaceuticals Limited | ANDA | View NDC → |
| 30 mg | Oral | Macleods Pharmaceuticals Limited | ANDA | View NDC → |
| 35 mg | Oral | Macleods Pharmaceuticals Limited | ANDA | View NDC → |
| 35 mg | Oral | Proficient Rx LP | ANDA | View NDC → |
| 5 mg | Oral | Sun Pharmaceutical Industries, Inc. | ANDA | View NDC → |
| 30 mg | Oral | Sun Pharmaceutical Industries, Inc. | ANDA | View NDC → |
| 35 mg | Oral | Sun Pharmaceutical Industries, Inc. | ANDA | View NDC → |
| 75 mg | Oral | Sun Pharmaceutical Industries, Inc. | ANDA | View NDC → |
| 150 mg | Oral | Sun Pharmaceutical Industries, Inc. | ANDA | View NDC → |
| 5 mg | Oral | Teva Pharmaceuticals USA, Inc. | ANDA | View NDC → |
| 30 mg | Oral | Teva Pharmaceuticals USA, Inc. | ANDA | View NDC → |
| 35 mg | Oral | Teva Pharmaceuticals USA, Inc. | ANDA | View NDC → |
Showing 21 of 21 products — FDA National Drug Code Directory. See every product, package size and price: browse all 21 Risedronate NDCs →
Risedronate side effects reported to the FDA (FAERS)
After a medicine reaches the market, patients, doctors and drugmakers can send the FDA reports of problems they think may be linked to it. Here’s what’s been reported for Risedronate — a signal of what to watch for, not proof the drug caused it.
Source: openFDA, from the FDA Adverse Event Reporting System (FAERS). These are voluntary reports — they don’t prove the drug caused the effect, and counts reflect how often something was reported, not how often it actually happens. Reports also often name the very problem the medicine is taken for — a common reason to file one is that the drug didn’t help — so for a pain reliever you may see “pain” high on the list; that points to why the report was filed, not to the drug causing the symptom. This counts every report that lists Risedronate in any role, so the total runs higher than the FDA’s official dashboard, which counts only cases where the drug is the suspect. For the authoritative figures, see the FDA FAERS Public Dashboard. Always talk to your pharmacist or doctor.
Risedronate FDA approval history
How Risedronate went from FDA review to the pharmacy shelf — the key milestones in its regulatory journey.
Source: Drugs@FDA.
Risedronate recall history
A recall is when a specific batch of a medicine is pulled from the market — usually a manufacturing issue, not a problem with the drug itself. Class I is most serious, Class III least.
The FDA’s enforcement reports list one Risedronate recall since July 2021. It is no longer listed as ongoing. A recall names specific lots from one company, so check the lot number on your own bottle rather than assuming every product is affected; your pharmacist can check whether your supply came from an affected lot.
- Risedronate Sodium Tablets, USP, 5 mg, Rx Only, 30-count bottle, Manufactured for: Macleods Pharma USA, Plainsboro, NJ 08536, Manufactured by: Macleods Pharmaceuticals Ltd., BAddi, HImchal Pradesh, I… Lots: Lot #: BRD2001A, Exp 5/2022 FDA record D-0762-2022 →
Source: FDA enforcement (recall) reports, via openFDA; our copy was last updated Sep 24, 2026.
RxNorm Concept Web — From Ingredient to Every Form and Strength
This page starts with one ingredient concept (IN). The branches below show its dose-form concepts (SCDF), then the available clinical drug and strength concepts (SCD). Combination products remain separate concepts with their own pages.
RxCUI 73056 2 dose forms · 6 strengths
-
Dose form (SCDF) Delayed Release Oral Tablet RxCUI 1020063In current FDA listingsClinical drug / strength (SCD) sodium 35 MGRxCUI 1020064 -
Dose form (SCDF) Oral Tablet RxCUI 617278In current FDA listingsClinical drug / strength (SCD) sodium 150 MGRxCUI 905028sodium 30 MGRxCUI 905032sodium 35 MGRxCUI 905024sodium 5 MGRxCUI 905041sodium 75 MGRxCUI 905083
Look up RxCUI 73056 in the RxCUI Atlas →
RxNorm is the U.S. National Library of Medicine’s normalized drug vocabulary. Its concept hierarchy can include forms that are not currently marketed; the status on each branch compares that concept with current FDA listings. RxCUIs identify vocabulary concepts, not individual packages or manufacturers.
Risedronate supply and shortage status
Whether Risedronate is in short supply in the U.S. right now, plus any shortage history the FDA has on record. A shortage usually reflects a manufacturing or demand issue — not a safety problem with the drug.
Source: openFDA, from the FDA Drug Shortages database.
💵 What Risedronate costs pharmacies (NADAC benchmark)
The national average invoice price pharmacies pay for the drug itself, from CMS's NADAC survey (data as of Sep 30, 2026). This is a supply-cost benchmark — not a retail price and not what you'd pay at the counter.
| Form | Strength | Pharmacy acquisition benchmark | |
|---|---|---|---|
| Tablet, Film Coated · Oral | 35 mg | $1.60 per tablet | NDC details & price history |
| Tablet, Film Coated · Oral | 5 mg | $1.52 per tablet | NDC details & price history |
| Tablet, Film Coated · Oral | 150 mg | $12.91 per tablet | NDC details & price history |
| Tablet, Delayed Release · Oral | 35 mg | $25.10 per tablet | NDC details & price history |
Source: CMS National Average Drug Acquisition Cost (NADAC), a survey of retail pharmacy invoice prices. Benchmarks shown are the range across package sizes of a representative product for each form and strength — other manufacturers' products may differ.
Risedronate brand names
Risedronate is sold under 2 brand names in the FDA directory — Actonel, Atelvia. A brand and its generic contain the same active ingredient; the brand name belongs to one company's product.
Who makes Risedronate: manufacturers and labelers
8 companies list Risedronate products with the FDA. By number of product records, the largest are Sun Pharmaceutical Industries, Inc., Aurobindo Pharma Limited, Apotex Corp.. Labelers include manufacturers and repackagers; the product in your bottle depends on which one your pharmacy stocks.
Sources for this Risedronate page
Core label, product, RxNorm, safety, and utilization data on this page come from the sources identified below. AI-written, editorial, and licensed sections are labeled separately.
How this page is built
HelloPharmacist combines public FDA and NLM records and does not author the underlying clinical facts. The plain-language sections are written with AI from the FDA-approved label text and reviewed by our pharmacy team before publication. Proficient Rx LP is the representative DailyMed label linked for verification and dates. This is general education, not medical advice: always talk to your doctor or pharmacist about your own medicines. How we build and review drug pages →