bisoprolol fumarate

Generic: bisoprolol fumarate

Labeler: advagen pharma ltd
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name bisoprolol fumarate
Generic Name bisoprolol fumarate
Labeler advagen pharma ltd
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

bisoprolol fumarate 10 mg/1

Manufacturer
Advagen Pharma Ltd

Identifiers & Regulatory

Product NDC 72888-093
Product ID 72888-093_43603823-594f-cbe7-e063-6294a90a9153
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075643
Listing Expiration 2026-12-31
Marketing Start 2000-11-16

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72888093
Hyphenated Format 72888-093

Supplemental Identifiers

RxCUI
854901 854905 865155
UPC
0372888093000 0372888093055 0372888092010 0372888092003 0372888093017 0372888092058 0372888233017 0372888092300 0372888093307
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
  • 10 mg/1
source: ndc
Packaging
  • 1000 TABLET, FILM COATED in 1 BOTTLE (72888-093-00)
  • 100 TABLET, FILM COATED in 1 BOTTLE (72888-093-01)
  • 500 TABLET, FILM COATED in 1 BOTTLE (72888-093-05)
  • 30 TABLET, FILM COATED in 1 BOTTLE (72888-093-30)
source: ndc

Packages (4)

72888-093-00 1000 TABLET, FILM COATED in 1 BOTTLE (72888-093-00) 72888-093-01 100 TABLET, FILM COATED in 1 BOTTLE (72888-093-01) 72888-093-05 500 TABLET, FILM COATED in 1 BOTTLE (72888-093-05) 72888-093-30 30 TABLET, FILM COATED in 1 BOTTLE (72888-093-30)

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": "43603823-594f-cbe7-e063-6294a90a9153", "openfda": {"upc": ["0372888093000", "0372888093055", "0372888092010", "0372888092003", "0372888093017", "0372888092058", "0372888233017", "0372888092300", "0372888093307"], "unii": ["UR59KN573L"], "rxcui": ["854901", "854905", "865155"], "spl_set_id": ["83e4b4e5-9130-44c8-abab-fcd0db5d8c49"], "manufacturer_name": ["Advagen Pharma Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (72888-093-00)", "package_ndc": "72888-093-00", "marketing_start_date": "20220701"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72888-093-01)", "package_ndc": "72888-093-01", "marketing_start_date": "20220701"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (72888-093-05)", "package_ndc": "72888-093-05", "marketing_start_date": "20220701"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72888-093-30)", "package_ndc": "72888-093-30", "marketing_start_date": "20220701"}], "brand_name": "Bisoprolol Fumarate", "product_id": "72888-093_43603823-594f-cbe7-e063-6294a90a9153", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72888-093", "generic_name": "Bisoprolol Fumarate", "labeler_name": "Advagen Pharma Ltd", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bisoprolol Fumarate", "active_ingredients": [{"name": "BISOPROLOL FUMARATE", "strength": "10 mg/1"}], "application_number": "ANDA075643", "marketing_category": "ANDA", "marketing_start_date": "20001116", "listing_expiration_date": "20261231"}