nebivolol

Generic: nebivolol hydrochloride

Labeler: avkare
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nebivolol
Generic Name nebivolol hydrochloride
Labeler avkare
Dosage Form TABLET
Routes
ORAL
Active Ingredients

nebivolol hydrochloride 2.5 mg/1

Manufacturer
AvKARE

Identifiers & Regulatory

Product NDC 42291-871
Product ID 42291-871_48842030-a03d-fb38-e063-6294a90a9dd0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203821
Listing Expiration 2027-12-31
Marketing Start 2024-07-10

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42291871
Hyphenated Format 42291-871

Supplemental Identifiers

RxCUI
387013 751612 751618 827073
UPC
0342291872905 0342291874909 0342291873902
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 hydrochloride (source: ndc)
Application Number ANDA203821 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (42291-871-30)
source: ndc

Packages (1)

42291-871-30 30 TABLET in 1 BOTTLE (42291-871-30)

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": "48842030-a03d-fb38-e063-6294a90a9dd0", "openfda": {"upc": ["0342291872905", "0342291874909", "0342291873902"], "unii": ["JGS34J7L9I"], "rxcui": ["387013", "751612", "751618", "827073"], "spl_set_id": ["1ce89dc5-018d-db40-e063-6294a90a9722"], "manufacturer_name": ["AvKARE"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (42291-871-30)", "package_ndc": "42291-871-30", "marketing_start_date": "20240710"}], "brand_name": "nebivolol", "product_id": "42291-871_48842030-a03d-fb38-e063-6294a90a9dd0", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "42291-871", "generic_name": "nebivolol hydrochloride", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "nebivolol", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA203821", "marketing_category": "ANDA", "marketing_start_date": "20240710", "listing_expiration_date": "20271231"}