nebivolol

Generic: nebivolol

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nebivolol
Generic Name nebivolol
Labeler aurobindo pharma limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

nebivolol hydrochloride 5 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 59651-138
Product ID 59651-138_8b2201ae-7174-45fe-a219-63d385d5c94b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211053
Listing Expiration 2026-12-31
Marketing Start 2021-12-17

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59651138
Hyphenated Format 59651-138

Supplemental Identifiers

RxCUI
387013 751612 751618 827073
UPC
0359651137307
UNII
JGS34J7L9I

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 nebivolol (source: ndc)
Generic Name nebivolol (source: ndc)
Application Number ANDA211053 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (59651-138-30)
  • 90 TABLET in 1 BOTTLE (59651-138-90)
source: ndc

Packages (2)

59651-138-30 30 TABLET in 1 BOTTLE (59651-138-30) 59651-138-90 90 TABLET in 1 BOTTLE (59651-138-90)

Ingredients (1)

nebivolol hydrochloride (5 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": "8b2201ae-7174-45fe-a219-63d385d5c94b", "openfda": {"upc": ["0359651137307"], "unii": ["JGS34J7L9I"], "rxcui": ["387013", "751612", "751618", "827073"], "spl_set_id": ["6e43a4e2-574e-4f4a-804d-e346b4edd2f1"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (59651-138-30)", "package_ndc": "59651-138-30", "marketing_start_date": "20211217"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (59651-138-90)", "package_ndc": "59651-138-90", "marketing_start_date": "20211217"}], "brand_name": "Nebivolol", "product_id": "59651-138_8b2201ae-7174-45fe-a219-63d385d5c94b", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "59651-138", "generic_name": "Nebivolol", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nebivolol", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA211053", "marketing_category": "ANDA", "marketing_start_date": "20211217", "listing_expiration_date": "20261231"}