HyVee Stimulant Laxative Bisacodyl 5 mg Tablet, 25-count
by HyVee Inc · 1 BLISTER PACK in 1 CARTON (42507-167-52) / 25 TABLET in 1 BLISTER PACK
NDC 42507-0167-52
🏷️ FDA NDC (as labeled)
42507-167-52
billing pads the product segment with a zero
This package
Contains25-count
Pack sizes2 compare ↓
Also comes in:
10 tablets 42507-0167-10
OTC
On market
Non-controlled
🗂️ Data synced Sep 17, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
🆔 Identity & classification
FDA NDC (as labeled)
42507-167-52
Product NDC
42507-167
11-digit billing NDC
42507016752
RxCUI
308753
UNII
10X0709Y6I
Application #
505G(a)(3)
SPL Set ID
495df989-a3c5-42ba-e063-6394a90ade2e
Established class (EPC)
Stimulant Laxative
Physiologic effect
Increased Large Intestinal Motility; Stimulation Large Intestine Fluid/Electrolyte Secretion
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2026-08-20
Route
ORAL
Dosage form
TABLET
Substance
BISACODYL
Why two NDCs?
The FDA registers this code as 42507-167-52 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 42507-0167-52. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.
🏷️ RxNorm drug class
This medicine belongs to the Stimulant Laxative class.
Pharmacologic class
Stimulant Laxative
Drug family (ATC)
Contact laxatives, Enemas
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.
🏭 Manufacturer & labeler
LabelerHyVee Inc
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code42507
First marketedAug 2026
Product typeHuman Otc Drug
Portfolio136 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.
🩺 Clinical
📗 Our plain-language guide HelloPharmacist
- It depends on which form you're using. Oral tablets (like Dulcolax Stimulant Laxative) usually take 6 to 12 hours, so many people take them at bedtime and get results in the mornin...
- No — it's really important not to chew, crush, or break bisacodyl tablets. They have a special protective coating that helps them reach the right part of your gut without irritatin...
- Can I chew or crush the tablet if I have trouble swallowing?
- Milk and antacids can break down the protective coating on bisacodyl tablets too soon, before the medicine reaches where it needs to work. This can cause stomach irritation and mak...
Patient education
Supplement & herbal interactions
Some supplements/herbs that may interact with Bisacodyl — tap one for details:
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.
💬 Questions about Bisacodyl?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
💊 What it looks like
Color
orange
ShapeRound
ImprintG
Size6 mm
ScoringNot scored
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.
🧪 Inactive Ingredients / Excipients
Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.
💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.
-
UNII 5C5403N26O
Acacia is a natural gum derived from acacia tree sap. It serves as a binder, thickener, and emulsifier to help hold ingredients together, improve texture, and stabilize the medicine.
-
UNII L11K75P92J
A mineral salt made from calcium and phosphate. It acts as a filler and binder in tablets to add bulk and help hold the medicine together in solid form.
-
UNII H0G9379FGK
Calcium carbonate is a white mineral powder used as a filler and buffering agent in medicines. It helps give tablets their bulk and size while neutralizing stomach acid in some formulations.
-
UNII M28OL1HH48
Croscarmellose sodium is a plant-based substance derived from cellulose. It acts as a disintegrant, helping tablets and capsules break down quickly in the digestive system so the medicine can be absorbed.
-
UNII 35SW5USQ3G
A synthetic yellow dye used to color medicines. It helps make tablets, capsules, and liquids visually distinct so patients can easily identify their medication.
-
UNII H77VEI93A8
A synthetic yellow dye used to color medications. It helps identify the drug and make it visually distinctive, with no effect on how the medicine works.
-
UNII 1K09F3G675
Ferric oxide red is an inorganic iron compound used as a colorant in medicines. It gives tablets, capsules, or other dosage forms a red or reddish tint for identification and appearance.
-
UNII 2G86QN327L
Gelatin is a protein derived from animal collagen, commonly used in medicines as a gelling agent and capsule material. It helps create soft or hard capsule shells that hold and release medication, and can also thicken liquid formulations.
-
UNII 230OU9XXE4
A waxy substance made from glycerin and stearic acid that acts as an emulsifier to blend oily and watery ingredients together. It also helps thicken and stabilize the medicine's texture.
-
UNII 3NXW29V3WO
Hypromellose is a plant-based thickener made from cellulose. It's used in medicines as a binder to hold ingredients together, a coating for tablets, and a thickener for liquids.
-
UNII 70097M6I30
Magnesium stearate is a salt made from magnesium and stearic acid, a fatty substance. It's used in tablets and capsules as a lubricant and glidant to help ingredients flow smoothly during manufacturing and prevent sticking.
-
UNII NX76LV5T8J
A synthetic plastic polymer made from methacrylic acid and ethyl acrylate. It's used as a coating or binder to control how and where the medicine dissolves in your digestive system.
-
UNII CR6K9C2NHK
A synthetic preservative derived from methylparaben. It prevents bacterial and fungal growth in medicines, extending shelf life and maintaining product safety during storage.
-
UNII OP1R32D61U
Microcrystalline cellulose is a purified form of cellulose, a natural fiber from plant sources. It acts as a binder and filler in tablets and capsules, helping hold ingredients together and give the medicine its shape and size.
-
UNII 3WJQ0SDW1A
Polyethylene glycol is a synthetic liquid or solid polymer used in medicines as a solvent, lubricant, and humectant. It helps dissolve active ingredients, reduces friction during manufacturing, and retains moisture in the final product.
-
UNII 625NNB0G9N
A preservative derived from benzoic acid that prevents bacterial and fungal growth in medicines. It helps keep the product safe and stable throughout its shelf life.
-
UNII ETJ7Z6XBU4
Silicon dioxide is a naturally occurring mineral used as a glidant and anti-caking agent. It helps powder ingredients flow smoothly and prevents clumping during manufacturing and storage.
-
UNII H8AV0SQX4D
A modified starch derived from potato or corn starch. It absorbs water quickly and helps tablets or capsules break apart and dissolve in the stomach, acting as a disintegrant to ensure the medicine releases its active ingredients properly.
-
UNII O8232NY3SJ
A plant-based carbohydrate derived from corn kernels. It acts as a filler to add bulk, a binder to hold ingredients together, and a disintegrant to help the tablet break apart in your stomach for absorption.
-
UNII C151H8M554
A natural sugar derived from sugar cane or sugar beets. It's used as a sweetener, filler, and binder to improve taste, add bulk, and help hold tablet or capsule ingredients together.
-
UNII 7SEV7J4R1U
A powder made from a naturally occurring mineral. In medicines, talc works as a glidant and anti-caking agent, helping tablets and capsules flow smoothly during manufacturing and preventing clumping.
-
UNII 15FIX9V2JP
Titanium dioxide is a bright white mineral powder commonly used as a colorant and opacifying agent. It makes pills and tablets white or lighter in color and helps make coatings non-transparent.
-
UNII 8Z96QXD6UM
Triethyl citrate is a clear liquid derived from citric acid. It acts as a plasticizer and solvent in tablet coatings and film formulations, helping the coating remain flexible and adhere properly to the medicine.
23 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statesacacia gum, calcium carbonate, croscarmellose sodium, D&C yellow no. 10, dibasic calcium phosphate, FD&C yellow no. 6, gelatin, glycerol monostearate, hypromellose, iron oxide red, magnesium stearate, methacrylic acid copolymer, microcrystalline cellulose, polyethylene glycol, precipitated silica, silicon dioxide, sodium methylparaben, sodium propylparaben, sodium starch glycolate, starch, sucrose, talc, titanium dioxide, triethyl citrate
Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.
Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed —
ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.Inactive ingredient FAQ
Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.
💲 Pricing
A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.
| Price system | Per each | Per package |
|---|---|---|
| Retail pharmacies payNADAC · weekly | Not in the retail survey — common for institutional, discontinued, or low-volume packs. | |
| Medicaid paysCMS SDUD · 12 mo | No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data. | |
| Medicare drug plans payPart D · quarterly | No Part D plan price is available for this NDC in our data. | |
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Try another pack size:
10 tablets
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.
🔁 Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Gentle Laxative 5 mg 70000-0538-01 | CARDINAL | 100 tablets | $0.044 | — | Availability likely | — |
| Womens Gentle Laxative 5 mg 11673-0151-52 | TARGET | 25 tablets | — | — | FDA listed | — |
| Womens Laxative Enteric Coated 5 mg 70000-0570-01 | CARDINAL | 25 tablets | — | — | FDA listed | — |
| SIMPEX Bisacodyl laxative 5 mg 76457-0003-00 | Simpex | 100 tablets | — | — | FDA listed | — |
| Stimulant Laxative Enteric Coated 5 mg 66424-0002-01 | SDA | 100 tablets | — | — | FDA listed | — |
| up and up gentle laxative 5 mg 11673-0116-25 | Target | 25 tablets | — | — | FDA listed | — |
| Dulcolax Stimulant Laxative 5 mg 41167-0200-01 | Chattem, | 10 tablets | — | — | FDA listed | — |
| Dulcolax Stimulant Laxative 5 mg 41167-0400-01 | Chattem, | 10 tablets | — | — | FDA listed | — |
| Womens Gentle Laxative 5 mg 69842-0089-52 | CVS | 25 tablets | — | — | FDA listed | — |
| GOOD REMEDIES GENTLE Laxative 5 mg 70692-0167-52 | Strive | 25 tablets | — | — | FDA listed | — |
| Bisacodyl 5 mg 72090-0131-01 | Pioneer | 300 tablets | — | — | FDA listed | — |
| stimulant laxative enteric coated 5 mg 57896-0441-01 | Geri-Care | 100 tablets | — | — | FDA listed | — |
| Dulcolax Simulant Laxative 5 mg 41167-0101-00 | Chattem, | 8 tablets | — | — | FDA listed | — |
| Bisacodyl 5 mg 41226-0003-52 | KROGER | 25 tablets | — | — | FDA listed | — |
| stimulant laxative enteric coated 5 mg 71335-1531-00 | Bryant | 25 tablets | — | — | FDA listed | — |
| stimulant laxative enteric coated 5 mg 85766-0148-00 | Sportpharm | 1000 tablets | — | — | FDA listed | — |
| Womens Laxative 5 mg 41226-0151-52 | KROGER | 25 tablets | — | — | FDA listed | — |
| Bisacodyl Stimulant Laxative 5 mg 68163-0116-25 | Raritan | 25 tablets | — | — | FDA listed | — |
| stimulant laxative enteric coated 5 mg 71610-0453-02 | Aphena | 2 tablets | — | — | FDA listed | — |
| Laxative 5 mg 37835-0241-01 | Bi-Mart | 100 tablets | — | — | FDA listed | — |
| Dulcolax Pink Stimulant Laxative 5 mg 41167-0290-05 | Chattem, | 25 tablets | — | — | FDA listed | — |
| Publix Stimulant Laxative 5 mg 41415-0116-25 | PUBLIX | 25 tablets | — | — | FDA listed | — |
| Womens Gentle Laxative 5 mg 21130-0555-30 | BETTER | 30 tablets | — | — | FDA listed | — |
| Gentle Laxative Stimulant Laxative 5 mg 63868-0908-25 | QUALITY | 25 tablets | — | — | FDA listed | — |
| Bisacodyl 5 mg 84324-0132-01 | NUVICARE | 100 tablets | — | — | FDA listed | — |
| RIGHT REMEDIES OVERNIGHT Laxative 5 mg 70692-0761-31 | Strive | 300 tablets | — | — | FDA listed | — |
| Fleet 5 mg 00132-0401-25 | C.B. | 25 tablets | — | — | FDA listed | — |
| Publix Women Laxative 5 mg 41415-0121-30 | PUBLIX | 30 tablets | — | — | FDA listed | — |
| HyVee Stimulant Laxative 5 mgthis 42507-0167-52 | HyVee | 25 tablets | — | — | FDA listed | — |
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.
⏳ Availability & generic status
🏛️
2026
On the market since
Aug 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found
We did not find an FDA-approved generic match for this exact strength, form and route.
Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.
🔬 Reported adverse events (FAERS)
Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Bisacodyl — the ingredient across all brands.
Top reported reactions
Age at onset
Reporter sex
Male · 43%
Female · 57%
Unknown · 0%
Serious outcomes
Reports over time (by year) — tap or hover for the count & year
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.
📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 42507-0167-10 | 1 BLISTER PACK in 1 CARTON (42507-167-10) / 10 TABLET in 1 BLISTER PACK | 2026-08-20 | Active |
| 42507-0167-52 You're viewing this | 1 BLISTER PACK in 1 CARTON (42507-167-52) / 25 TABLET in 1 BLISTER PACK | 2026-08-20 | Active |
Pack size FAQ
What quantity is in NDC 42507-0167-52?
NDC 42507-0167-52 is a 25-count package — 1 blister pack in 1 carton / 25 tablet in 1 blister pack.
What is the difference between NDC 42507-0167-52 and NDC 42507-0167-10?
Both are HyVee Stimulant Laxative Bisacodyl 5 mg Tablet — the drug itself is identical. NDC 42507-0167-52 is the 25-count package, while NDC 42507-0167-10 is the 10 tablets package.
What NDC number is used to bill for this package of HyVee Stimulant Laxative Bisacodyl 5 mg Tablet?
Bill NDC 42507-0167-52 — the 11-digit billing format is 42507016752. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.
🧭 About this NDC listing & data coverage
Over-the-counter (OTC) product
What data is (and isn’t) available for this NDC — tap to expand
| NDC identity (package / product / labeler codes) | ✓ Available |
| Labeler | ✓ Available |
| Product & package description | ✓ Available |
| Marketing category & status | ✓ Available |
| Active ingredient / dosage form / route | ✓ Available |
| FDA label (SPL via DailyMed) | ✓ Available |
| Package photos | ✓ Available |
| Inactive ingredients (structured) | ✓ Available |
| NADAC pharmacy acquisition price (CMS) | — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey. |
| Orange Book / therapeutic-equivalence data | — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope. |
| HCPCS J-code billing crosswalk | — Not published for this NDC Most self-administered / retail products have no J-code — that is normal. |
| Medicaid utilization (CMS SDUD) | — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold. |
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.
Questions about this listing
Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The FDA registers it as 42507-167-52, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 42507-0167-52, written without dashes as 42507016752. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 42507-0167-52, the first segment (42507) is the labeler code FDA assigned to HyVee Inc; the middle segment (0167) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (52) identifies this exact package size and type. Together they name one specific package of one specific product.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by HyVee Inc. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 10 tablets (42507-0167-10). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
HyVee Inc is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.
📄 FDA label — Drug Facts FDA SPL
The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage
⏱️ Dosage and Administration
⚠️ Warnings
📦 Storage and Handling
🧪 Active Ingredient
🧪 Inactive Ingredients
🎯 Purpose
🎯 Indications and Usage ▾
Use • for relief of occasional constipation and irregularity • this product generally produces bowel movement in 6 to 12 hours
⏱️ Dosage and Administration ▾
Directions • do not take more than directed • take with a glass of water
⚠️ Warnings ▾
Warnings Do not use • if you cannot swallow without chewing. Ask a doctor before use if you have • stomach pain, nausea or vomiting • noticed a sudden change in bowel habits that lasts more than 2 weeks When using this product • it may cause stomach discomfort, faintness and cramps • do not chew or crush tablet(s) • do not use within 1 hour after taking an antacid or milk Stop use and ask a doctor if • you have rectal bleeding or fail to have a bowel movement after using this product. These could be signs of a serious condition. • you need to use a laxative for more than 1 week If pregnant or breast-feeding , ask a health professional before use.
Keep out of reach of children. Overdose warning In case of overdose, get medical help or contact a Poison Control Center right away.
📦 Storage and Handling ▾
Other information • contains FD&C yellow no. 6 • store at 20-25°C (68-77°F) • protect from light, heat and moisture
🧪 Active Ingredient ▾
Active ingredient (in each tablet) Bisacodyl USP 5 mg
🧪 Inactive Ingredients ▾
Inactive ingredients acacia gum, calcium carbonate, croscarmellose sodium, D&C yellow no. 10, dibasic calcium phosphate, FD&C yellow no. 6, gelatin, glycerol monostearate, hypromellose, iron oxide red, magnesium stearate, methacrylic acid copolymer, microcrystalline cellulose, polyethylene glycol, precipitated silica, silicon dioxide, sodium methylparaben, sodium propylparaben, sodium starch glycolate, starch, sucrose, talc, titanium dioxide, triethyl citrate
🎯 Purpose ▾
Purpose Stimulant laxative
No label section mentions that — try another word, or open the full label on DailyMed below.
Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA.
Prefer the government’s original formatting? View this label on DailyMed ↗
For educational and professional reference only — not medical advice. Pricing reflects published
NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.