bisoprolol fumarate

Generic: bisoprolol fumarate

Labeler: rising pharma holdings, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name bisoprolol fumarate
Generic Name bisoprolol fumarate
Labeler rising pharma holdings, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

bisoprolol fumarate 5 mg/1

Manufacturer
Rising Pharma Holdings, Inc.

Identifiers & Regulatory

Product NDC 64980-709
Product ID 64980-709_520db5c6-f4f3-4574-a36b-5a548f61a344
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA219044
Listing Expiration 2026-12-31
Marketing Start 2025-07-11

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 64980709
Hyphenated Format 64980-709

Supplemental Identifiers

RxCUI
854901 854905
UPC
0364980710015 0364980709019
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 ANDA219044 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (64980-709-01)
  • 30 TABLET, FILM COATED in 1 BOTTLE (64980-709-03)
source: ndc

Packages (2)

64980-709-01 100 TABLET, FILM COATED in 1 BOTTLE (64980-709-01) 64980-709-03 30 TABLET, FILM COATED in 1 BOTTLE (64980-709-03)

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": "520db5c6-f4f3-4574-a36b-5a548f61a344", "openfda": {"upc": ["0364980710015", "0364980709019"], "unii": ["UR59KN573L"], "rxcui": ["854901", "854905"], "spl_set_id": ["200ab93b-6ad3-46cb-8f57-db056a14de16"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (64980-709-01)", "package_ndc": "64980-709-01", "marketing_start_date": "20250711"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (64980-709-03)", "package_ndc": "64980-709-03", "marketing_start_date": "20250711"}], "brand_name": "Bisoprolol Fumarate", "product_id": "64980-709_520db5c6-f4f3-4574-a36b-5a548f61a344", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "64980-709", "generic_name": "Bisoprolol Fumarate", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bisoprolol Fumarate", "active_ingredients": [{"name": "BISOPROLOL FUMARATE", "strength": "5 mg/1"}], "application_number": "ANDA219044", "marketing_category": "ANDA", "marketing_start_date": "20250711", "listing_expiration_date": "20261231"}