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Metoprolol Tartrate 100 mg Tablet, Film Coated, 90-count — NDC 72789-0595-90 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Metoprolol Tartrate 100 mg Tablet, Film Coated, 90-count — NDC 72789-595-90 (Billing 72789-0595-90)

by PD-Rx Pharmaceuticals, Inc. · 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

This is a package of 90 tablets of Metoprolol Tartrate 100 mg Tablet, Film Coated from PD-Rx Pharmaceuticals, Inc., marketed since Dec 1993 and currently FDA-listed. It is this product's only package size.

NDC 72789-0595-90
🏷️ FDA NDC (as labeled) 72789-595-90 billing pads the product segment with a zero
Rx only Generic On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Oct 1, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

⚠️
Other active recalls for Metoprolol Tartrate (different manufacturers) — 1 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · May 6, 2024 — Presence of Foreign Substance: metal in tablet (Rubicon Research Private Limited) · FDA recall D-0517-2024
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 72789-595-90
Product NDC 72789-595
11-digit billing NDC 72789059590
Application # ANDA076704
SPL Set ID 39d822df-0fa4-4f06-a6f1-d313824c62df
Established class (EPC) beta-Adrenergic Blocker
Mechanism of action Adrenergic beta-Antagonists
DEA schedule Non-controlled
Marketing category ANDA
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 1993-12-23
Route ORAL
Dosage form TABLET, FILM COATED
Substance METOPROLOL TARTRATE
TE code (Orange Book) AB · RLD · RS
Why two NDCs? The FDA registers this code as 72789-595-90 — 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 → 72789-0595-90. 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.

Clinical

📗 Our plain-language guide HelloPharmacist
  • It depends on which form you have. Metoprolol tartrate and Lopressor tablets treat high blood pressure and angina, and lower the risk of death after a heart attack. Metoprolol succ...
  • Take it exactly as prescribed. Tartrate tablets go with or right after a meal. Extended-release succinate tablets are taken once daily and should not be crushed or chewed. Ask your...
  • Please don't stop suddenly. Stopping abruptly can make angina worse and has led to heart attacks. Even if you only take it for blood pressure, your doctor will lower the dose gradu...
  • Tiredness, dizziness, a slow heartbeat, low blood pressure, diarrhea, itching or rash are the more common ones. Most were mild and temporary. Call your doctor if you faint, your he...
📖 Read our full Metoprolol guide →

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
1
Nutrient depletion considerations

Metoprolol may be associated with lower levels of 1 nutrient — worth a chat with your pharmacist, not a cause for alarm.

🧪 Full Metoprolol nutrient depletion report →
An association is not a deficiency. Educational only — don't start or stop anything without professional guidance.
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.

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 systemPer eachPer 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.
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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
72789-0595-90 You're viewing this Main listing 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 2026-09-28 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Metoprolol Tartrate 100 mg 62584-0267-01 American 1 tablet $0.029 AB Availability likely —
Metoprolol Tartrate 100 mg 52817-0254-00 TRUPHARMA 1000 tablets $0.029 AB Availability likely —
Metoprolol Tartrate 100 mg 68645-0191-59 Legacy 60 tablets $0.029 AB Availability likely —
Metoprolol Tartrate 100 mg 57237-0102-01 Rising 100 tablets $0.029 AB Availability likely —
Metoprolol Tartrate 100 mg 65862-0064-01 Aurobindo 100 tablets $0.029 AB Availability likely —
Metoprolol Tartrate 100 mg 00378-0047-01 Mylan 100 tablets $0.029 AB Availability likely —
Metoprolol Tartrate 100 mg 76282-0796-01 Exelan 100 tablets $0.029 AB Availability likely —
Metoprolol Tartrate 100 mg 52817-0362-00 TruPharma 1000 tablets $0.029 AB Availability likely —
Metoprolol Tartrate 100 mg 72888-0006-00 Advagen 1000 tablets $0.029 AB Availability likely —
Metoprolol Tartrate 100 mg 72888-0212-00 Advagen 1000 tablets $0.029 AB Availability likely —
Metoprolol Tartrate 100 mg 60760-0566-90 St. 90 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 63187-0532-30 Proficient 30 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 71610-0080-53 Aphena 60 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 71610-0186-53 Aphena 60 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 71610-0559-53 Aphena 60 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 82804-0979-00 Proficient 100 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 50090-7488-00 A-S 90 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 70518-3793-00 REMEDYREPACK 30 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 68071-3935-01 NuCare 120 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 69367-0355-01 Westminster 100 tablets — AB Discontinued —
Metoprolol Tartrate 100 mg 71335-9716-01 Bryant 30 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 50090-7570-00 A-S 90 tablets — AB FDA listed —
Lopressor 100 mg 30698-0459-01 Validus 100 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 50090-6764-00 A-S 90 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 50090-7740-00 A-S 30 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 68071-4958-01 NuCare 100 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 87063-0188-01 ASCLEMED 100 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 51407-0111-01 Golden 100 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 60760-0928-90 ST. 90 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 72189-0544-30 Direct_Rx 30 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 76420-0954-00 Asclemed 1000 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 43063-0938-30 PD-Rx 30 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 53401-0012-60 Aphena 90 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 55154-2126-00 Cardinal 1 tablet — AB FDA listed —
Metoprolol Tartrate 100 mg 70518-4535-00 REMEDYREPACK 30 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 50090-1974-00 A-S 30 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 50090-6763-00 A-S 30 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 50090-7741-00 A-S 90 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 68071-4880-01 NuCare 120 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 71335-2675-01 Bryant 30 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 51655-0884-52 Northwind 30 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 53401-0017-60 Aphena 90 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 68071-3941-06 NuCare 60 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 68788-8885-01 Preferred 100 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 70518-3997-00 REMEDYREPACK 180 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 50090-2260-00 A-S 30 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 50090-7569-00 A-S 30 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 51655-0514-25 Northwind 60 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 68788-8249-01 Preferred 100 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 67046-1626-03 Coupler 30 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 71335-1157-01 Bryant 30 tablets — AB Discontinued —
Metoprolol Tartrate 100 mg 72189-0659-90 Direct_Rx 90 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 82804-0313-30 Proficient 30 tablets — AB FDA listed —
Metoprolol Tartrate 100 mg 70518-4748-00 REMEDYREPACK 30 tablets — AB FDA listed —
Metoprolol Tartrate 100 mgthis 72789-0595-90 PD-Rx 90 tablets — AB FDA listed —
About this product: this is a generic version of the medicine. FDA equivalence ratings are shown when available, and other versions are listed above, least expensive first.
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

🏛️
1993
On the market since
Dec 1993
📍
2026
Currently FDA-listed
33 years listed
🔓
·
Generic on the market
this product is a generic
✅This is a generic drug

This product is an FDA-approved generic. Other versions of the same drug are listed under Therapeutic equivalents, least expensive first.

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.

What it looks like

Color blue
ShapeRound
ImprintM;47
Size1 mm
ScoringScored — splits in 2
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 3SY5LH9PMK
    Anhydrous lactose is a milk sugar with no water content. It acts as a filler and binder in tablets and capsules, adding bulk and helping ingredients stick together.
  • 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 L06K8R7DQK
    A synthetic blue dye approved by the FDA for use in medications and foods. It serves as a colorant to make pills and liquids visually distinct and easier to identify.
  • UNII 9H4L916OBU
    Hypromellose 2208 is a plant-derived cellulose that thickens and forms protective coats. It's used in medications as a binder to hold ingredients together and as a coating to control how fast the medicine dissolves.
  • UNII 1IVH67816N
    Hypromellose 2910 is a plant-derived cellulose compound used as a thickener and film-former in medicines. It helps control how quickly the medication dissolves and creates protective coatings on tablets or capsules.
  • UNII 0WZ8WG20P6
    Hypromellose 2910 is a plant-based cellulose derivative that acts as a thickener, binder, and film-coating agent. It helps control how quickly the medicine dissolves and protects the tablet or capsule from moisture and light.
  • 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 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 VH2XOU12IE
    Polydextrose is a synthetic polymer made from dextrose (sugar) that acts as a bulking agent and filler in medicines. It helps give tablets and capsules proper volume and texture while often adding slight sweetness.
  • UNII B697894SGQ
    Polyethylene glycol 400 is a clear, thick liquid made from petroleum-derived polymers. It acts as a solvent and humectant in medicines, helping dissolve active ingredients and retain moisture in the formulation.
  • UNII Q662QK8M3B
    Polyethylene glycol 8000 is a synthetic polymer made from ethylene oxide. It acts as a binder and filler in tablets and capsules, helping hold ingredients together and add bulk to the medicine.
  • UNII FZ989GH94E
    Povidone is a synthetic polymer made from a plastic-like material. It acts as a binder to hold tablet ingredients together and as a disintegrant to help the tablet break apart in your stomach so the medicine can be absorbed.
  • 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 368GB5141J
    A detergent and foaming agent derived from coconut or palm oil. In medications, it helps break down and mix oil and water-based ingredients, aids in tablet disintegration, and improves how the drug dissolves and spreads in the mouth or digestive system.
  • 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 XHX3C3X673
    Triacetin is a clear, oily liquid made from glycerin and acetic acid. It works as a plasticizer and solvent in medicines, helping soften coatings and improve how liquids mix together in formulations.

16 inactive ingredients listed in the exact product block matched to this NDC.

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.

Manufacturer & labeler

LabelerPD-Rx Pharmaceuticals, Inc.
Application holderMYLAN PHARMACEUTICALS INC
FDA applicationANDA076704 (ANDA)
Labeler code72789
First marketedDec 1993
Product typeHuman Prescription Drug
Portfolio834 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.

Full prescribing information FDA SPL

The complete FDA label for this product — the official prescribing information, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
📄 FDA label
📄 FDA label 19 words ▾

No FDA label is on file for this product yet. Labels load from openFDA / DailyMed and refresh weekly.

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

Medicare Part D spend CMS · PART D · 2026 (Q1)

Medicare Part D (outpatient prescription) spending for Metoprolol Tartrate — the program that covers self-administered drugs. 13 manufacturers.
⚠️ Drug-level data: CMS publishes Part D spending by drug, not by NDC — these figures combine every manufacturer, strength and package size sold under the name Metoprolol Tartrate. That’s a different level of aggregation than the Medicaid card above, which is specific to this exact 11-digit NDC (pack size included), so the two aren’t directly comparable.
Period
Total Part D spend
$27.2M
Claims incl. refills
3.6M
Beneficiaries
2.6M
Spend / beneficiary
$10.52
Spend / claim
$7.50
Trend by period
💵 About the dollar figures: spending is what Part D plans paid before confidential manufacturer rebates, so the program’s real net cost is lower. A blank patient count means fewer than 11 people — CMS hides counts that small to protect privacy. Source: CMS Medicare Quarterly Part D Spending by Drug (data.cms.gov), updated quarterly.

About this NDC listing & data coverage

Finished prescription 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 ✓ Available
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

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 form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
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 PD-Rx Pharmaceuticals, Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
PD-Rx Pharmaceuticals, 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 a prescription product, so it is dispensed under a prescriber's order. Your pharmacist can tell you whether any over-the-counter forms of the same medication exist.
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.
← 72789-0593-90 · PD-Rx 72789-0596-90 · PD-Rx →
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.