nebivolol

Generic: nebivolol hydrochloride

Labeler: apnar pharma lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nebivolol
Generic Name nebivolol hydrochloride
Labeler apnar pharma lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

nebivolol hydrochloride 2.5 mg/1

Manufacturer
Apnar Pharma LP

Identifiers & Regulatory

Product NDC 24689-159
Product ID 24689-159_ffc06b5e-4f7d-4020-8be9-a4e903c1bfa8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216568
Listing Expiration 2026-12-31
Marketing Start 2024-05-13

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 24689159
Hyphenated Format 24689-159

Supplemental Identifiers

RxCUI
387013 751612 751618 827073
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 ANDA216568 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (24689-159-01)
  • 90 TABLET in 1 BOTTLE (24689-159-02)
source: ndc

Packages (2)

24689-159-01 30 TABLET in 1 BOTTLE (24689-159-01) 24689-159-02 90 TABLET in 1 BOTTLE (24689-159-02)

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": "ffc06b5e-4f7d-4020-8be9-a4e903c1bfa8", "openfda": {"unii": ["JGS34J7L9I"], "rxcui": ["387013", "751612", "751618", "827073"], "spl_set_id": ["3f5766c0-e1fa-4805-a32c-523182310ad5"], "manufacturer_name": ["Apnar Pharma LP"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (24689-159-01)", "package_ndc": "24689-159-01", "marketing_start_date": "20240513"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (24689-159-02)", "package_ndc": "24689-159-02", "marketing_start_date": "20240513"}], "brand_name": "nebivolol", "product_id": "24689-159_ffc06b5e-4f7d-4020-8be9-a4e903c1bfa8", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "24689-159", "generic_name": "nebivolol hydrochloride", "labeler_name": "Apnar Pharma LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "nebivolol", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA216568", "marketing_category": "ANDA", "marketing_start_date": "20240513", "listing_expiration_date": "20261231"}