metoprolol tartrate

Generic: metoprolol tartrate

Labeler: asclemed usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol tartrate
Generic Name metoprolol tartrate
Labeler asclemed usa, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

metoprolol tartrate 50 mg/1

Manufacturer
Asclemed USA, Inc.

Identifiers & Regulatory

Product NDC 76420-953
Product ID 76420-953_30a06de6-ded3-748c-e063-6294a90afb0f
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 76420953
Hyphenated Format 76420-953

Supplemental Identifiers

RxCUI
866511 866514 866924
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
  • 1000 TABLET, FILM COATED in 1 BOTTLE (76420-953-00)
  • 100 TABLET, FILM COATED in 1 BOTTLE (76420-953-01)
  • 20 TABLET, FILM COATED in 1 BOTTLE (76420-953-20)
  • 30 TABLET, FILM COATED in 1 BOTTLE (76420-953-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE (76420-953-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE (76420-953-90)
source: ndc

Packages (6)

76420-953-00 1000 TABLET, FILM COATED in 1 BOTTLE (76420-953-00) 76420-953-01 100 TABLET, FILM COATED in 1 BOTTLE (76420-953-01) 76420-953-20 20 TABLET, FILM COATED in 1 BOTTLE (76420-953-20) 76420-953-30 30 TABLET, FILM COATED in 1 BOTTLE (76420-953-30) 76420-953-60 60 TABLET, FILM COATED in 1 BOTTLE (76420-953-60) 76420-953-90 90 TABLET, FILM COATED in 1 BOTTLE (76420-953-90)

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": "30a06de6-ded3-748c-e063-6294a90afb0f", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866511", "866514", "866924"], "spl_set_id": ["e3de56de-b707-405e-bf97-837070e5c744"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (76420-953-00)", "package_ndc": "76420-953-00", "marketing_start_date": "20250318"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (76420-953-01)", "package_ndc": "76420-953-01", "marketing_start_date": "20250318"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (76420-953-20)", "package_ndc": "76420-953-20", "marketing_start_date": "20250318"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (76420-953-30)", "package_ndc": "76420-953-30", "marketing_start_date": "20250318"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (76420-953-60)", "package_ndc": "76420-953-60", "marketing_start_date": "20250318"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (76420-953-90)", "package_ndc": "76420-953-90", "marketing_start_date": "20250318"}], "brand_name": "Metoprolol Tartrate", "product_id": "76420-953_30a06de6-ded3-748c-e063-6294a90afb0f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "76420-953", "generic_name": "Metoprolol Tartrate", "labeler_name": "Asclemed USA, Inc.", "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"}