nebivolol
Generic: nebivolol
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
nebivolol
Generic Name
nebivolol
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
nebivolol hydrochloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
63629-9424
Product ID
63629-9424_ebf0662a-eab8-48c6-8601-78198caec5b2
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA211053
Listing Expiration
2026-12-31
Marketing Start
2021-12-17
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
636299424
Hyphenated Format
63629-9424
Supplemental Identifiers
RxCUI
UNII
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
ANDA211053 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (63629-9424-1)
- 90 TABLET in 1 BOTTLE (63629-9424-2)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ebf0662a-eab8-48c6-8601-78198caec5b2", "openfda": {"unii": ["JGS34J7L9I"], "rxcui": ["751612"], "spl_set_id": ["ef3b8ec9-0cec-40d4-824f-fc2b6cafd39a"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (63629-9424-1)", "package_ndc": "63629-9424-1", "marketing_start_date": "20220816"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (63629-9424-2)", "package_ndc": "63629-9424-2", "marketing_start_date": "20220816"}], "brand_name": "Nebivolol", "product_id": "63629-9424_ebf0662a-eab8-48c6-8601-78198caec5b2", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "63629-9424", "generic_name": "Nebivolol", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nebivolol", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA211053", "marketing_category": "ANDA", "marketing_start_date": "20211217", "listing_expiration_date": "20261231"}