nebivolol

Generic: nebivolol

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

Drug Facts

Product Profile

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

nebivolol hydrochloride 2.5 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-2415
Product ID 72162-2415_2124870a-c883-46ee-8f1d-bcb1c01ef301
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208717
Listing Expiration 2026-12-31
Marketing Start 2017-12-29

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721622415
Hyphenated Format 72162-2415

Supplemental Identifiers

RxCUI
751618
UNII
JGS34J7L9I

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 ANDA208717 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (72162-2415-3)
source: ndc

Packages (1)

72162-2415-3 30 TABLET in 1 BOTTLE (72162-2415-3)

Ingredients (1)

nebivolol hydrochloride (2.5 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": "2124870a-c883-46ee-8f1d-bcb1c01ef301", "openfda": {"unii": ["JGS34J7L9I"], "rxcui": ["751618"], "spl_set_id": ["abb0546f-08dd-4354-8b41-d17065b52c24"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72162-2415-3)", "package_ndc": "72162-2415-3", "marketing_start_date": "20241031"}], "brand_name": "Nebivolol", "product_id": "72162-2415_2124870a-c883-46ee-8f1d-bcb1c01ef301", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72162-2415", "generic_name": "Nebivolol", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nebivolol", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA208717", "marketing_category": "ANDA", "marketing_start_date": "20171229", "listing_expiration_date": "20261231"}