bisoprolol fumarate

Generic: bisoprolol fumarate

Labeler: unichem pharmaceuticals (usa), inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name bisoprolol fumarate
Generic Name bisoprolol fumarate
Labeler unichem pharmaceuticals (usa), inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

bisoprolol fumarate 10 mg/1

Manufacturer
Unichem Pharmaceuticals (USA), Inc.

Identifiers & Regulatory

Product NDC 29300-127
Product ID 29300-127_958d523d-b040-4475-ad89-6278e5cf0f60
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078635
Listing Expiration 2026-12-31
Marketing Start 2009-09-21

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 29300127
Hyphenated Format 29300-127

Supplemental Identifiers

RxCUI
854901 854905
UPC
0329300126136 0329300127133
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 ANDA078635 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (29300-127-01)
  • 500 TABLET in 1 BOTTLE, PLASTIC (29300-127-05)
  • 30 TABLET in 1 BOTTLE, PLASTIC (29300-127-13)
source: ndc

Packages (3)

29300-127-01 100 TABLET in 1 BOTTLE, PLASTIC (29300-127-01) 29300-127-05 500 TABLET in 1 BOTTLE, PLASTIC (29300-127-05) 29300-127-13 30 TABLET in 1 BOTTLE, PLASTIC (29300-127-13)

Ingredients (1)

bisoprolol fumarate (10 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": "958d523d-b040-4475-ad89-6278e5cf0f60", "openfda": {"upc": ["0329300126136", "0329300127133"], "unii": ["UR59KN573L"], "rxcui": ["854901", "854905"], "spl_set_id": ["4f20df45-3f9c-4a91-b394-e93a08111ec3"], "manufacturer_name": ["Unichem Pharmaceuticals (USA), Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (29300-127-01)", "package_ndc": "29300-127-01", "marketing_start_date": "20090921"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (29300-127-05)", "package_ndc": "29300-127-05", "marketing_start_date": "20160819"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (29300-127-13)", "package_ndc": "29300-127-13", "marketing_start_date": "20090921"}], "brand_name": "Bisoprolol Fumarate", "product_id": "29300-127_958d523d-b040-4475-ad89-6278e5cf0f60", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "29300-127", "generic_name": "Bisoprolol fumarate", "labeler_name": "Unichem Pharmaceuticals (USA), Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bisoprolol Fumarate", "active_ingredients": [{"name": "BISOPROLOL FUMARATE", "strength": "10 mg/1"}], "application_number": "ANDA078635", "marketing_category": "ANDA", "marketing_start_date": "20090921", "listing_expiration_date": "20261231"}