bisoprolol fumarate

Generic: bisoprolol fumarate

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name bisoprolol fumarate
Generic Name bisoprolol fumarate
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

bisoprolol fumarate 5 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8671
Product ID 68788-8671_2eb410f7-87a6-4402-9bce-925be3d3c946
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078635
Listing Expiration 2026-12-31
Marketing Start 2024-05-21

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687888671
Hyphenated Format 68788-8671

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
  • 100 TABLET in 1 BOTTLE, PLASTIC (68788-8671-1)
source: ndc

Packages (1)

Ingredients (1)

bisoprolol fumarate (5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2eb410f7-87a6-4402-9bce-925be3d3c946", "openfda": {"unii": ["UR59KN573L"], "rxcui": ["854905"], "spl_set_id": ["c0e309f3-82c3-4629-b790-fb8538b87369"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (68788-8671-1)", "package_ndc": "68788-8671-1", "marketing_start_date": "20240521"}], "brand_name": "Bisoprolol Fumarate", "product_id": "68788-8671_2eb410f7-87a6-4402-9bce-925be3d3c946", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68788-8671", "generic_name": "Bisoprolol fumarate", "labeler_name": "Preferred Pharmaceuticals Inc.", "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": "20240521", "listing_expiration_date": "20261231"}