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 100 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7740
Product ID 50090-7740_8b2702ee-da84-4d0f-a87f-bb800a7b99fe
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200981
Listing Expiration 2026-12-31
Marketing Start 2018-12-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907740
Hyphenated Format 50090-7740

Supplemental Identifiers

RxCUI
866511
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 ANDA200981 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-7740-0)
  • 60 TABLET, FILM COATED in 1 BOTTLE (50090-7740-1)
  • 90 TABLET, FILM COATED in 1 BOTTLE (50090-7740-3)
  • 180 TABLET, FILM COATED in 1 BOTTLE (50090-7740-4)
source: ndc

Packages (4)

50090-7740-0 30 TABLET, FILM COATED in 1 BOTTLE (50090-7740-0) 50090-7740-1 60 TABLET, FILM COATED in 1 BOTTLE (50090-7740-1) 50090-7740-3 90 TABLET, FILM COATED in 1 BOTTLE (50090-7740-3) 50090-7740-4 180 TABLET, FILM COATED in 1 BOTTLE (50090-7740-4)

Ingredients (1)

metoprolol tartrate (100 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": "8b2702ee-da84-4d0f-a87f-bb800a7b99fe", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866511"], "spl_set_id": ["3911c18b-1259-4c6d-9466-73372eb7bd81"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-7740-0)", "package_ndc": "50090-7740-0", "marketing_start_date": "20251029"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-7740-1)", "package_ndc": "50090-7740-1", "marketing_start_date": "20251029"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7740-3)", "package_ndc": "50090-7740-3", "marketing_start_date": "20251029"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (50090-7740-4)", "package_ndc": "50090-7740-4", "marketing_start_date": "20251029"}], "brand_name": "METOPROLOL TARTRATE", "product_id": "50090-7740_8b2702ee-da84-4d0f-a87f-bb800a7b99fe", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-7740", "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": "100 mg/1"}], "application_number": "ANDA200981", "marketing_category": "ANDA", "marketing_start_date": "20181201", "listing_expiration_date": "20261231"}