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 5 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2516
Product ID 71335-2516_afe4a662-64fe-49a5-a45c-2bee2070ef85
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212682
Listing Expiration 2026-12-31
Marketing Start 2022-02-14

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 713352516
Hyphenated Format 71335-2516

Supplemental Identifiers

RxCUI
387013
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
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-2516-1)
  • 90 TABLET in 1 BOTTLE (71335-2516-2)
source: ndc

Packages (2)

71335-2516-1 30 TABLET in 1 BOTTLE (71335-2516-1) 71335-2516-2 90 TABLET in 1 BOTTLE (71335-2516-2)

Ingredients (1)

nebivolol (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": "afe4a662-64fe-49a5-a45c-2bee2070ef85", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["030Y90569U"], "rxcui": ["387013"], "spl_set_id": ["126de78c-fb3d-4a53-9aaf-f2dfe1ac2a2f"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2516-1)", "package_ndc": "71335-2516-1", "marketing_start_date": "20241024"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2516-2)", "package_ndc": "71335-2516-2", "marketing_start_date": "20241024"}], "brand_name": "NEBIVOLOL", "product_id": "71335-2516_afe4a662-64fe-49a5-a45c-2bee2070ef85", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71335-2516", "generic_name": "nebivolol", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NEBIVOLOL", "active_ingredients": [{"name": "NEBIVOLOL", "strength": "5 mg/1"}], "application_number": "ANDA212682", "marketing_category": "ANDA", "marketing_start_date": "20220214", "listing_expiration_date": "20261231"}