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Metoprolol Tartrate 50 mg Tablet, 30-count — NDC 68071-3946-3 (Billing 68071-3946-03)

by NuCare Pharmaceuticals,Inc. · 30 TABLET in 1 BOTTLE

This is a package of 30 tablets of Metoprolol Tartrate 50 mg Tablet from NuCare Pharmaceuticals,Inc., marketed since Jan 2024 and currently FDA-listed.

NDC 68071-3946-03
🏷️ FDA NDC (as labeled) 68071-3946-3 billing pads the package segment with a zero
This package
Contains30-count Pack sizes4 compare ↓
Also priced by: Part D plans $0.0707/unit — full pricing hub ↓
Rx only Generic On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Oct 8, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

NDC database record

One package, one record: these facts belong to NDC 68071-3946-3 alone.

Record
FDA NDC Directory package listing · Human prescription drug
Code segments
68071 labeler · 3946 product · 3 package
Package marketed since
Apr 16, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 6807139463 4
FDA record last changed
Oct 8, 2026
⚠️
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) 68071-3946-3
Product NDC 68071-3946
11-digit billing NDC 68071394603
Application # ANDA200981
SPL Set ID 5b9d9ac4-3cf3-3822-e063-6394a90a8b9a
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 2024-01-17
Route ORAL
Dosage form TABLET
Substance METOPROLOL TARTRATE
TE code (Orange Book) AB · RLD · RS
Why two NDCs? The FDA registers this code as 68071-3946-3 — a 5-4-1 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 package segment → 68071-3946-03. 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

📖 What it is MedlinePlus · NLM

Metoprolol is used to treat high blood pressure, angina (chest pain) and heart failure. Metoprolol also is used to improve survival after a heart attack . Metoprolol is in a class of medications called beta blockers. It works by relaxing blood vessels and slowing heart rate to improve blood flow and decrease blood pressure.

Read the full MedlinePlus article ↗
📗 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 →
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.

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 · Q2 2026 $0.0707 $2.12 / 30 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
68071-3946-03 You're viewing this 30 TABLET in 1 BOTTLE 2026-04-16 — Active
68071-3946-09 68071-3946-9 90 TABLET in 1 BOTTLE 2026-06-11 — Active
68071-3946-01 68071-3946-1 Main listing 120 TABLET in 1 BOTTLE 2026-06-11 — Active
68071-3946-08 68071-3946-8 180 TABLET in 1 BOTTLE 2026-09-16 — Active

You're viewing the smallest of 4 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This is a 30-count package — 30 tablet in 1 bottle.
How does this package differ from NDC 68071-3946-09?
Both are Metoprolol Tartrate 50 mg Tablet — the drug itself is identical. This page's package is the 30-count one, while NDC 68071-3946-09 is the 90 tablets package.
What NDC number is used to bill for this package of Metoprolol Tartrate 50 mg Tablet?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Metoprolol Tartrate 50 mg 00378-0032-01 Mylan 100 tablets $0.019 AB Availability likely —
Metoprolol Tartrate 50 mg 51079-0801-20 Mylan 1 tablet $0.019 AB Availability likely —
Metoprolol Tartrate 50 mg 52817-0252-00 TRUPHARMA 1000 tablets $0.019 AB Availability likely —
Metoprolol Tartrate 50 mg 52817-0361-00 TruPharma 1000 tablets $0.019 AB Availability likely —
Metoprolol Tartrate 50 mg 57237-0101-01 Rising 100 tablets $0.019 AB Availability likely —
Metoprolol Tartrate 50 mg 62584-0266-01 American 1 tablet $0.019 AB Availability likely —
Metoprolol Tartrate 50 mg 65862-0063-01 Aurobindo 100 tablets $0.019 AB Availability likely —
Metoprolol Tartrate 50 mg 68645-0190-59 Legacy 60 tablets $0.019 AB Availability likely —
Metoprolol Tartrate 50 mg 72888-0005-00 Advagen 1000 tablets $0.019 AB Availability likely —
Metoprolol Tartrate 50 mg 72888-0210-00 Advagen 1000 tablets $0.019 AB Availability likely —
Metoprolol Tartrate 50 mg 76282-0795-01 Exelan 100 tablets $0.019 AB Availability likely —
Lopressor 50 mg 30698-0458-01 Validus 100 tablets $2.416 AB Availability likely —
Metoprolol Tartrate 50 mg 00615-8422-05 NCS 15 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 42708-0041-60 QPharma 60 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 42708-0147-60 QPharma, 60 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 42708-0198-60 QPharma, 60 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 43063-0821-30 PD-Rx 30 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 46708-0291-10 Alembic 100 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 48433-0074-20 Safecor 1 tablet — AB FDA listed —
Metoprolol Tartrate 50 mg 50090-1979-00 A-S 30 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 50090-2149-00 A-S 30 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 50090-5060-00 A-S 90 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 50090-6076-00 A-S 90 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 50090-6083-00 A-S 30 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 50090-6084-00 A-S 90 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 50090-7553-00 A-S 30 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 50090-7554-00 A-S 90 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 50090-7969-00 A-S 30 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 50090-7970-00 A-S 90 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 51407-0110-01 Golden 100 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 51655-0281-25 Northwind 60 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 51655-0527-25 Northwind 60 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 53401-0016-60 Aphena 90 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 55154-4790-00 Cardinal 1 tablet — AB FDA listed —
Metoprolol Tartrate 50 mg 55154-5512-00 Cardinal 1 tablet — AB FDA listed —
Metoprolol Tartrate 50 mg 60760-0524-60 St. 60 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 60760-0680-60 St. 60 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 62332-0113-30 Alembic 30 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 63187-0609-00 Proficient 100 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 67046-1569-03 Coupler 30 tablets — AB FDA listed —
Metoprolol Tartrate 50 mgthis 68071-3946-03 NuCare 30 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 68071-3985-08 NuCare 180 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 68071-4755-02 NuCare 120 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 68071-4769-01 NuCare 100 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 68071-4957-01 NuCare 100 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 68788-7548-01 Preferred 100 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 68788-8211-01 Preferred 100 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 68788-8886-01 Preferred 100 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 69367-0354-01 Westminster 100 tablets — AB Discontinued —
Metoprolol Tartrate 50 mg 70518-3293-00 REMEDYREPACK 60 tablets — AB Discontinued —
Metoprolol Tartrate 50 mg 70518-4418-00 REMEDYREPACK 30 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 70882-0133-60 Cambridge 60 tablets — AB Discontinued —
Metoprolol Tartrate 50 mg 71205-0701-30 Proficient 30 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 71335-1146-01 Bryant 100 tablets — AB Discontinued —
Metoprolol Tartrate 50 mg 71335-2164-01 Bryant 100 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 71335-2656-01 Bryant 100 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 71610-0138-60 Aphena 90 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 71610-0147-60 Aphena 90 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 71610-0565-30 Aphena 30 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 72189-0677-90 Direct_Rx 90 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 72789-0535-90 PD-Rx 90 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 72789-0549-93 PD-Rx 180 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 72789-0555-90 PD-Rx 90 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 76420-0953-00 Asclemed 1000 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 82804-0165-90 Proficient 90 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 82804-0253-30 Proficient 30 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 82804-0978-00 Proficient 100 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 82868-0090-30 Northwind 30 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 87063-0186-01 ASCLEMED 100 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 55154-0278-00 Cardinal 1 tablet — AB FDA listed —
Metoprolol Tartrate 50 mg 72789-0583-60 PD-Rx 60 tablets — AB FDA listed —
Metoprolol Tartrate 50 mg 67296-2322-03 Redpharm 30 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

🏛️
2024
On the market since
Jan 2024
📍
2026
Currently FDA-listed
2 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.

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.

🧪 Avoiding an ingredient? See Metoprolol inactive ingredients by manufacturer: every current product's list side by side, so you can ask your pharmacy for the version that does not list it.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

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

LabelerNuCare Pharmaceuticals,Inc.
Application holderRUBICON RESEARCH LTD
FDA applicationANDA200981 (ANDA)
Labeler code68071
First marketedJan 2024
Product typeHuman Prescription Drug
Portfolio1,015 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 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 — Not published for this NDC No photo available yet for this listing.
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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 NuCare Pharmaceuticals,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 3 other package presentations of this same product, including 90 tablets (68071-3946-09), 120 tablets (68071-3946-01), 180 tablets (68071-3946-08). 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?
NuCare 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.
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.