nebivolol

Generic: nebivolol

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nebivolol
Generic Name nebivolol
Labeler american health packaging
Dosage Form TABLET
Routes
ORAL
Active Ingredients

nebivolol hydrochloride 10 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-652
Product ID 60687-652_35420d8c-7a05-0220-e063-6394a90a1c25
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203828
Listing Expiration 2026-12-31
Marketing Start 2022-09-07

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687652
Hyphenated Format 60687-652

Supplemental Identifiers

RxCUI
387013 751612
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 ANDA203828 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 BLISTER PACK in 1 CARTON (60687-652-21) / 1 TABLET in 1 BLISTER PACK (60687-652-11)
source: ndc

Packages (1)

60687-652-21 30 BLISTER PACK in 1 CARTON (60687-652-21) / 1 TABLET in 1 BLISTER PACK (60687-652-11)

Ingredients (1)

nebivolol hydrochloride (10 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": "35420d8c-7a05-0220-e063-6394a90a1c25", "openfda": {"unii": ["JGS34J7L9I"], "rxcui": ["387013", "751612"], "spl_set_id": ["5418f2b2-3e23-4e7a-b4df-36a1515c9a12"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (60687-652-21)  / 1 TABLET in 1 BLISTER PACK (60687-652-11)", "package_ndc": "60687-652-21", "marketing_start_date": "20220907"}], "brand_name": "Nebivolol", "product_id": "60687-652_35420d8c-7a05-0220-e063-6394a90a1c25", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "60687-652", "generic_name": "Nebivolol", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nebivolol", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA203828", "marketing_category": "ANDA", "marketing_start_date": "20220907", "listing_expiration_date": "20261231"}