metoprolol tartrate

Generic: metoprolol tartrate

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol tartrate
Generic Name metoprolol tartrate
Labeler bryant ranch prepack
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

metoprolol tartrate 100 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1157
Product ID 71335-1157_bf81fdaa-a3e3-46d6-a8a2-3d9c6c508777
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200981
Listing Expiration 2026-12-31
Marketing Start 2018-12-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713351157
Hyphenated Format 71335-1157

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, FILM COATED in 1 BOTTLE (71335-1157-1)
  • 100 TABLET, FILM COATED in 1 BOTTLE (71335-1157-2)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71335-1157-3)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71335-1157-4)
  • 180 TABLET, FILM COATED in 1 BOTTLE (71335-1157-5)
source: ndc

Packages (5)

71335-1157-1 30 TABLET, FILM COATED in 1 BOTTLE (71335-1157-1) 71335-1157-2 100 TABLET, FILM COATED in 1 BOTTLE (71335-1157-2) 71335-1157-3 60 TABLET, FILM COATED in 1 BOTTLE (71335-1157-3) 71335-1157-4 90 TABLET, FILM COATED in 1 BOTTLE (71335-1157-4) 71335-1157-5 180 TABLET, FILM COATED in 1 BOTTLE (71335-1157-5)

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": "bf81fdaa-a3e3-46d6-a8a2-3d9c6c508777", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866511"], "spl_set_id": ["bf81fdaa-a3e3-46d6-a8a2-3d9c6c508777"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-1157-1)", "package_ndc": "71335-1157-1", "marketing_start_date": "20190508"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-1157-2)", "package_ndc": "71335-1157-2", "marketing_start_date": "20200109"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-1157-3)", "package_ndc": "71335-1157-3", "marketing_start_date": "20190319"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-1157-4)", "package_ndc": "71335-1157-4", "marketing_start_date": "20190822"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (71335-1157-5)", "package_ndc": "71335-1157-5", "marketing_start_date": "20190318"}], "brand_name": "Metoprolol Tartrate", "product_id": "71335-1157_bf81fdaa-a3e3-46d6-a8a2-3d9c6c508777", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71335-1157", "generic_name": "Metoprolol Tartrate", "labeler_name": "Bryant Ranch Prepack", "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": "20181201", "listing_expiration_date": "20261231"}