bisoprolol fumarate

Generic: bisoprolol fumarate

Labeler: trupharma llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name bisoprolol fumarate
Generic Name bisoprolol fumarate
Labeler trupharma llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

bisoprolol fumarate 2.5 mg/1

Manufacturer
TruPharma LLC

Identifiers & Regulatory

Product NDC 52817-268
Product ID 52817-268_32f899b9-1d84-7c3d-e063-6394a90a502c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075643
Listing Expiration 2026-12-31
Marketing Start 2025-03-07

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 52817268
Hyphenated Format 52817-268

Supplemental Identifiers

RxCUI
865155
UPC
0352817268303
UNII
UR59KN573L

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 bisoprolol fumarate (source: ndc)
Generic Name bisoprolol fumarate (source: ndc)
Application Number ANDA075643 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (52817-268-30)
source: ndc

Packages (1)

52817-268-30 30 TABLET, FILM COATED in 1 BOTTLE (52817-268-30)

Ingredients (1)

bisoprolol fumarate (2.5 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": "32f899b9-1d84-7c3d-e063-6394a90a502c", "openfda": {"upc": ["0352817268303"], "unii": ["UR59KN573L"], "rxcui": ["865155"], "spl_set_id": ["0ef9e45c-21ee-4e00-a9b8-280e2035b4d3"], "manufacturer_name": ["TruPharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (52817-268-30)", "package_ndc": "52817-268-30", "marketing_start_date": "20250307"}], "brand_name": "Bisoprolol Fumarate", "product_id": "52817-268_32f899b9-1d84-7c3d-e063-6394a90a502c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "52817-268", "generic_name": "Bisoprolol Fumarate", "labeler_name": "TruPharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bisoprolol Fumarate", "active_ingredients": [{"name": "BISOPROLOL FUMARATE", "strength": "2.5 mg/1"}], "application_number": "ANDA075643", "marketing_category": "ANDA", "marketing_start_date": "20250307", "listing_expiration_date": "20261231"}