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 50 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-1979
Product ID 50090-1979_213d34c0-3a02-4408-8ed7-d3d91e8ed9c3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077739
Listing Expiration 2027-12-31
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 500901979
Hyphenated Format 50090-1979

Supplemental Identifiers

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

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-1979-0)
  • 60 TABLET, FILM COATED in 1 BOTTLE (50090-1979-1)
  • 90 TABLET, FILM COATED in 1 BOTTLE (50090-1979-4)
  • 180 TABLET, FILM COATED in 1 BOTTLE (50090-1979-5)
source: ndc

Packages (4)

50090-1979-0 30 TABLET, FILM COATED in 1 BOTTLE (50090-1979-0) 50090-1979-1 60 TABLET, FILM COATED in 1 BOTTLE (50090-1979-1) 50090-1979-4 90 TABLET, FILM COATED in 1 BOTTLE (50090-1979-4) 50090-1979-5 180 TABLET, FILM COATED in 1 BOTTLE (50090-1979-5)

Ingredients (1)

metoprolol tartrate (50 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": "213d34c0-3a02-4408-8ed7-d3d91e8ed9c3", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866511", "866514"], "spl_set_id": ["e1bb16fa-4f72-44bc-bc33-d7653c13f55c"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-1979-0)", "package_ndc": "50090-1979-0", "marketing_start_date": "20190701"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-1979-1)", "package_ndc": "50090-1979-1", "marketing_start_date": "20150910"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-1979-4)", "package_ndc": "50090-1979-4", "marketing_start_date": "20150910"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (50090-1979-5)", "package_ndc": "50090-1979-5", "marketing_start_date": "20150910"}], "brand_name": "Metoprolol Tartrate", "product_id": "50090-1979_213d34c0-3a02-4408-8ed7-d3d91e8ed9c3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-1979", "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": "50 mg/1"}], "application_number": "ANDA077739", "marketing_category": "ANDA", "marketing_start_date": "20070911", "listing_expiration_date": "20271231"}