nebivolol

Generic: nebivolol

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nebivolol
Generic Name nebivolol
Labeler major pharmaceuticals
Dosage Form TABLET
Routes
ORAL
Active Ingredients

nebivolol 10 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-7499
Product ID 0904-7499_d4d0a3fd-6520-4358-acce-8ecb76bfd8f7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212682
Listing Expiration 2026-12-31
Marketing Start 2025-02-24

Pharmacologic Class

Established (EPC)
beta-adrenergic blocker [epc]
Mechanism of Action
adrenergic beta-antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09047499
Hyphenated Format 0904-7499

Supplemental Identifiers

RxCUI
387013 751612 751618
UNII
030Y90569U
NUI
N0000000161 N0000175556

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 nebivolol (source: ndc)
Generic Name nebivolol (source: ndc)
Application Number ANDA212682 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 BLISTER PACK in 1 CARTON (0904-7499-04) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

0904-7499-04 30 BLISTER PACK in 1 CARTON (0904-7499-04) / 1 TABLET in 1 BLISTER PACK

Ingredients (1)

nebivolol (10 mg/1)

Linked Drug Pages (1)

NEBIVOLOL ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d4d0a3fd-6520-4358-acce-8ecb76bfd8f7", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["030Y90569U"], "rxcui": ["387013", "751612", "751618"], "spl_set_id": ["3e9e1048-b5ea-4d6a-9363-3ee0d059e088"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (0904-7499-04)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-7499-04", "marketing_start_date": "20250224"}], "brand_name": "NEBIVOLOL", "product_id": "0904-7499_d4d0a3fd-6520-4358-acce-8ecb76bfd8f7", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "0904-7499", "generic_name": "nebivolol", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NEBIVOLOL", "active_ingredients": [{"name": "NEBIVOLOL", "strength": "10 mg/1"}], "application_number": "ANDA212682", "marketing_category": "ANDA", "marketing_start_date": "20250224", "listing_expiration_date": "20261231"}