bisoprolol fumarate

Generic: bisoprolol fumarate

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name bisoprolol fumarate
Generic Name bisoprolol fumarate
Labeler american health packaging
Dosage Form TABLET
Routes
ORAL
Active Ingredients

bisoprolol fumarate 5 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-679
Product ID 60687-679_253e530d-88da-d032-e063-6394a90a7641
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078635
Listing Expiration 2026-12-31
Marketing Start 2023-04-20

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687679
Hyphenated Format 60687-679

Supplemental Identifiers

RxCUI
854905
UNII
UR59KN573L

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 bisoprolol fumarate (source: ndc)
Generic Name bisoprolol fumarate (source: ndc)
Application Number ANDA078635 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 BLISTER PACK in 1 CARTON (60687-679-21) / 1 TABLET in 1 BLISTER PACK (60687-679-11)
source: ndc

Packages (1)

60687-679-21 30 BLISTER PACK in 1 CARTON (60687-679-21) / 1 TABLET in 1 BLISTER PACK (60687-679-11)

Ingredients (1)

bisoprolol fumarate (5 mg/1)

Linked Drug Pages (1)

Bisoprolol Fumarate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "253e530d-88da-d032-e063-6394a90a7641", "openfda": {"unii": ["UR59KN573L"], "rxcui": ["854905"], "spl_set_id": ["36b53e7f-e306-40a8-8d1b-d00695a4fe61"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (60687-679-21)  / 1 TABLET in 1 BLISTER PACK (60687-679-11)", "package_ndc": "60687-679-21", "marketing_start_date": "20230420"}], "brand_name": "Bisoprolol Fumarate", "product_id": "60687-679_253e530d-88da-d032-e063-6394a90a7641", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "60687-679", "generic_name": "Bisoprolol fumarate", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bisoprolol Fumarate", "active_ingredients": [{"name": "BISOPROLOL FUMARATE", "strength": "5 mg/1"}], "application_number": "ANDA078635", "marketing_category": "ANDA", "marketing_start_date": "20230420", "listing_expiration_date": "20261231"}