bisoprolol fumarate

Generic: bisoprolol fumarate

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

Drug Facts

Product Profile

Brand Name bisoprolol fumarate
Generic Name bisoprolol fumarate
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

bisoprolol fumarate 5 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2178
Product ID 71335-2178_93041a9f-53d9-47b4-96d7-d2b138ea1b06
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215563
Listing Expiration 2026-12-31
Marketing Start 2021-10-29

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713352178
Hyphenated Format 71335-2178

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 ANDA215563 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-2178-1)
  • 100 TABLET in 1 BOTTLE (71335-2178-2)
  • 90 TABLET in 1 BOTTLE (71335-2178-3)
  • 28 TABLET in 1 BOTTLE (71335-2178-4)
  • 120 TABLET in 1 BOTTLE (71335-2178-5)
source: ndc

Packages (5)

71335-2178-1 30 TABLET in 1 BOTTLE (71335-2178-1) 71335-2178-2 100 TABLET in 1 BOTTLE (71335-2178-2) 71335-2178-3 90 TABLET in 1 BOTTLE (71335-2178-3) 71335-2178-4 28 TABLET in 1 BOTTLE (71335-2178-4) 71335-2178-5 120 TABLET in 1 BOTTLE (71335-2178-5)

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": "93041a9f-53d9-47b4-96d7-d2b138ea1b06", "openfda": {"unii": ["UR59KN573L"], "rxcui": ["854905"], "spl_set_id": ["f6ce8f14-43fc-4c5e-8378-62ca7121e918"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2178-1)", "package_ndc": "71335-2178-1", "marketing_start_date": "20221017"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-2178-2)", "package_ndc": "71335-2178-2", "marketing_start_date": "20221017"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2178-3)", "package_ndc": "71335-2178-3", "marketing_start_date": "20221017"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-2178-4)", "package_ndc": "71335-2178-4", "marketing_start_date": "20221017"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-2178-5)", "package_ndc": "71335-2178-5", "marketing_start_date": "20221017"}], "brand_name": "Bisoprolol Fumarate", "product_id": "71335-2178_93041a9f-53d9-47b4-96d7-d2b138ea1b06", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71335-2178", "generic_name": "Bisoprolol Fumarate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bisoprolol Fumarate", "active_ingredients": [{"name": "BISOPROLOL FUMARATE", "strength": "5 mg/1"}], "application_number": "ANDA215563", "marketing_category": "ANDA", "marketing_start_date": "20211029", "listing_expiration_date": "20261231"}