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 50090-6076
Product ID 50090-6076_3beeda9c-62fa-4175-8b05-2dc51dd1d137
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 500906076
Hyphenated Format 50090-6076

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 ANDA077739 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE (50090-6076-0)
source: ndc

Packages (1)

50090-6076-0 90 TABLET, FILM COATED in 1 BOTTLE (50090-6076-0)

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": "3beeda9c-62fa-4175-8b05-2dc51dd1d137", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866514"], "spl_set_id": ["2a42adef-5af9-439e-a796-72bbd8a1748f"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6076-0)", "package_ndc": "50090-6076-0", "marketing_start_date": "20220915"}], "brand_name": "Metoprolol Tartrate", "product_id": "50090-6076_3beeda9c-62fa-4175-8b05-2dc51dd1d137", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-6076", "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": "20261231"}