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
Routes
ORAL
Active Ingredients

metoprolol tartrate 50 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-0488
Product ID 50090-0488_fcfe4d3e-fcd9-46e5-a628-d1b7629923cb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074644
Listing Expiration 2026-12-31
Marketing Start 2015-06-29

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500900488
Hyphenated Format 50090-0488

Supplemental Identifiers

RxCUI
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 ANDA074644 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-0488-0)
  • 60 TABLET in 1 BOTTLE (50090-0488-1)
  • 90 TABLET in 1 BOTTLE (50090-0488-4)
  • 180 TABLET in 1 BOTTLE (50090-0488-5)
source: ndc

Packages (4)

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": "fcfe4d3e-fcd9-46e5-a628-d1b7629923cb", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866514"], "spl_set_id": ["822d80cc-3c46-4e10-94bc-9b5fe5a4c22d"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-0488-0)", "package_ndc": "50090-0488-0", "marketing_start_date": "20160629"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-0488-1)", "package_ndc": "50090-0488-1", "marketing_start_date": "20160629"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-0488-4)", "package_ndc": "50090-0488-4", "marketing_start_date": "20160629"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (50090-0488-5)", "package_ndc": "50090-0488-5", "marketing_start_date": "20160629"}], "brand_name": "Metoprolol tartrate", "product_id": "50090-0488_fcfe4d3e-fcd9-46e5-a628-d1b7629923cb", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-0488", "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": "ANDA074644", "marketing_category": "ANDA", "marketing_start_date": "20150629", "listing_expiration_date": "20261231"}