metoprolol tartrate

Generic: metoprolol tartrate

Labeler: westminster pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol tartrate
Generic Name metoprolol tartrate
Labeler westminster pharmaceuticals, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

metoprolol tartrate 100 mg/1

Manufacturer
Westminster Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 69367-355
Product ID 69367-355_451f6d3f-6a31-fb28-e063-6294a90a06a0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074453
Marketing Start 2023-12-18
Marketing End 2026-07-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69367355
Hyphenated Format 69367-355

Supplemental Identifiers

RxCUI
866511 866514
UPC
0369367355018 0369367354103 0369367354011
UNII
W5S57Y3A5L

Packaging Origin

Original Packager
true

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 ANDA074453 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (69367-355-01)
  • 1000 TABLET in 1 BOTTLE (69367-355-10)
source: ndc

Packages (2)

69367-355-01 100 TABLET in 1 BOTTLE (69367-355-01) 69367-355-10 1000 TABLET in 1 BOTTLE (69367-355-10)

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": "451f6d3f-6a31-fb28-e063-6294a90a06a0", "openfda": {"upc": ["0369367355018", "0369367354103", "0369367354011"], "unii": ["W5S57Y3A5L"], "rxcui": ["866511", "866514"], "spl_set_id": ["4d352c34-47f8-4662-9ac5-d5a32bd1660f"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69367-355-01)", "package_ndc": "69367-355-01", "marketing_end_date": "20260731", "marketing_start_date": "20231218"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (69367-355-10)", "package_ndc": "69367-355-10", "marketing_end_date": "20260731", "marketing_start_date": "20231218"}], "brand_name": "METOPROLOL TARTRATE", "product_id": "69367-355_451f6d3f-6a31-fb28-e063-6294a90a06a0", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "69367-355", "generic_name": "metoprolol tartrate", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METOPROLOL TARTRATE", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "100 mg/1"}], "application_number": "ANDA074453", "marketing_category": "ANDA", "marketing_end_date": "20260731", "marketing_start_date": "20231218"}