metoprolol tartrate

Generic: metoprolol tartrate

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol tartrate
Generic Name metoprolol tartrate
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

metoprolol tartrate 25 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7363
Product ID 50090-7363_c4ee814e-352b-4f8b-8aa0-c7084b3ab6b8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077739
Listing Expiration 2026-12-31
Marketing Start 2007-09-11

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907363
Hyphenated Format 50090-7363

Supplemental Identifiers

RxCUI
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
  • 25 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE (50090-7363-0)
source: ndc

Packages (1)

50090-7363-0 90 TABLET, FILM COATED in 1 BOTTLE (50090-7363-0)

Ingredients (1)

metoprolol tartrate (25 mg/1)

Linked Drug Pages (1)

Metoprolol Tartrate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c4ee814e-352b-4f8b-8aa0-c7084b3ab6b8", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866924"], "spl_set_id": ["771c262d-e1db-4a75-9609-110c27c43e51"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7363-0)", "package_ndc": "50090-7363-0", "marketing_start_date": "20241018"}], "brand_name": "Metoprolol Tartrate", "product_id": "50090-7363_c4ee814e-352b-4f8b-8aa0-c7084b3ab6b8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-7363", "generic_name": "Metoprolol Tartrate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Tartrate", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "25 mg/1"}], "application_number": "ANDA077739", "marketing_category": "ANDA", "marketing_start_date": "20070911", "listing_expiration_date": "20261231"}