metoprolol tartrate

Generic: metoprolol

Labeler: northwind health company, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol tartrate
Generic Name metoprolol
Labeler northwind health company, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

metoprolol tartrate 50 mg/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 82868-090
Product ID 82868-090_471cc93d-6d30-bf85-e063-6294a90abc87
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202871
Listing Expiration 2026-12-31
Marketing Start 2025-10-07

Pharmacologic Class

Classes
adrenergic beta-antagonists [moa] beta-adrenergic blocker [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82868090
Hyphenated Format 82868-090

Supplemental Identifiers

RxCUI
866514
UNII
W5S57Y3A5L

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name metoprolol tartrate (source: ndc)
Generic Name metoprolol (source: ndc)
Application Number ANDA202871 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (82868-090-30)
source: ndc

Packages (1)

Ingredients (1)

metoprolol tartrate (50 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "471cc93d-6d30-bf85-e063-6294a90abc87", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866514"], "spl_set_id": ["471ccbfe-96dd-7ab9-e063-6394a90a5bd6"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (82868-090-30)", "package_ndc": "82868-090-30", "marketing_start_date": "20251007"}], "brand_name": "METOPROLOL TARTRATE", "product_id": "82868-090_471cc93d-6d30-bf85-e063-6294a90abc87", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "82868-090", "generic_name": "METOPROLOL", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METOPROLOL TARTRATE", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "50 mg/1"}], "application_number": "ANDA202871", "marketing_category": "ANDA", "marketing_start_date": "20251007", "listing_expiration_date": "20261231"}