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 50090-2260
Product ID 50090-2260_b988019e-ae73-4ec7-be08-e9ef6a3f96ed
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 500902260
Hyphenated Format 50090-2260

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
  • 100 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-2260-0)
  • 60 TABLET, FILM COATED in 1 BOTTLE (50090-2260-1)
  • 90 TABLET, FILM COATED in 1 BOTTLE (50090-2260-3)
  • 180 TABLET, FILM COATED in 1 BOTTLE (50090-2260-4)
source: ndc

Packages (4)

50090-2260-0 30 TABLET, FILM COATED in 1 BOTTLE (50090-2260-0) 50090-2260-1 60 TABLET, FILM COATED in 1 BOTTLE (50090-2260-1) 50090-2260-3 90 TABLET, FILM COATED in 1 BOTTLE (50090-2260-3) 50090-2260-4 180 TABLET, FILM COATED in 1 BOTTLE (50090-2260-4)

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": "b988019e-ae73-4ec7-be08-e9ef6a3f96ed", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866511", "866514", "866924"], "spl_set_id": ["f4e88ecc-2d9b-4bad-97dd-77b1cbb75eb0"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-2260-0)", "package_ndc": "50090-2260-0", "marketing_start_date": "20151209"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-2260-1)", "package_ndc": "50090-2260-1", "marketing_start_date": "20151209"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-2260-3)", "package_ndc": "50090-2260-3", "marketing_start_date": "20151209"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (50090-2260-4)", "package_ndc": "50090-2260-4", "marketing_start_date": "20151209"}], "brand_name": "Metoprolol Tartrate", "product_id": "50090-2260_b988019e-ae73-4ec7-be08-e9ef6a3f96ed", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-2260", "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": "ANDA077739", "marketing_category": "ANDA", "marketing_start_date": "20070911", "listing_expiration_date": "20261231"}