metoprolol tartrate

Generic: metoprolol tartrate

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol tartrate
Generic Name metoprolol tartrate
Labeler american health packaging
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

metoprolol tartrate 50 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 62584-266
Product ID 62584-266_2e966478-1706-ae7a-e063-6394a90a9a8e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077739
Listing Expiration 2026-12-31
Marketing Start 2010-06-22

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62584266
Hyphenated Format 62584-266

Supplemental Identifiers

RxCUI
866511 866514 866924
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 tartrate (source: ndc)
Application Number ANDA077739 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 BOX, UNIT-DOSE (62584-266-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (62584-266-11)
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": "2e966478-1706-ae7a-e063-6394a90a9a8e", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866511", "866514", "866924"], "spl_set_id": ["0a3ccfd4-8b65-4c7e-b0ba-27ff40d5b5e8"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (62584-266-01)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (62584-266-11)", "package_ndc": "62584-266-01", "marketing_start_date": "20100622"}], "brand_name": "Metoprolol Tartrate", "product_id": "62584-266_2e966478-1706-ae7a-e063-6394a90a9a8e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "62584-266", "generic_name": "Metoprolol Tartrate", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Tartrate", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "50 mg/1"}], "application_number": "ANDA077739", "marketing_category": "ANDA", "marketing_start_date": "20100622", "listing_expiration_date": "20261231"}