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 100 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7569
Product ID 50090-7569_eece7874-2c59-42b1-8cae-470666e1afab
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200981
Listing Expiration 2026-12-31
Marketing Start 2024-01-17

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907569
Hyphenated Format 50090-7569

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 in 1 BOTTLE (50090-7569-0)
  • 60 TABLET in 1 BOTTLE (50090-7569-1)
  • 90 TABLET in 1 BOTTLE (50090-7569-3)
  • 180 TABLET in 1 BOTTLE (50090-7569-4)
source: ndc

Packages (4)

Ingredients (1)

metoprolol tartrate (100 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "eece7874-2c59-42b1-8cae-470666e1afab", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866511"], "spl_set_id": ["a2add754-0bd9-4f8a-ae05-b06d35d7f423"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-7569-0)", "package_ndc": "50090-7569-0", "marketing_start_date": "20250604"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-7569-1)", "package_ndc": "50090-7569-1", "marketing_start_date": "20250604"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7569-3)", "package_ndc": "50090-7569-3", "marketing_start_date": "20250604"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (50090-7569-4)", "package_ndc": "50090-7569-4", "marketing_start_date": "20250604"}], "brand_name": "METOPROLOL TARTRATE", "product_id": "50090-7569_eece7874-2c59-42b1-8cae-470666e1afab", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-7569", "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": "20240117", "listing_expiration_date": "20261231"}