nebivolol

Generic: nebivolol

Labeler: ani pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nebivolol
Generic Name nebivolol
Labeler ani pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

nebivolol hydrochloride 2.5 mg/1

Manufacturer
ANI Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 62559-275
Product ID 62559-275_4bca2b49-cd1c-4645-99e7-511dd1b67da6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203659
Listing Expiration 2026-12-31
Marketing Start 2021-09-17

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62559275
Hyphenated Format 62559-275

Supplemental Identifiers

RxCUI
387013 751612 751618 827073
UPC
0362559275309 0362559276306 0362559278300 0362559277303
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 (source: ndc)
Application Number ANDA203659 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (62559-275-30)
  • 2300 TABLET in 1 BOTTLE (62559-275-83)
source: ndc

Packages (2)

62559-275-30 30 TABLET in 1 BOTTLE (62559-275-30) 62559-275-83 2300 TABLET in 1 BOTTLE (62559-275-83)

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": "4bca2b49-cd1c-4645-99e7-511dd1b67da6", "openfda": {"upc": ["0362559275309", "0362559276306", "0362559278300", "0362559277303"], "unii": ["JGS34J7L9I"], "rxcui": ["387013", "751612", "751618", "827073"], "spl_set_id": ["3ebcc539-efe0-4545-bd83-37c20de7efb0"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (62559-275-30)", "package_ndc": "62559-275-30", "marketing_start_date": "20210917"}, {"sample": false, "description": "2300 TABLET in 1 BOTTLE (62559-275-83)", "package_ndc": "62559-275-83", "marketing_start_date": "20210917"}], "brand_name": "Nebivolol", "product_id": "62559-275_4bca2b49-cd1c-4645-99e7-511dd1b67da6", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "62559-275", "generic_name": "Nebivolol", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nebivolol", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA203659", "marketing_category": "ANDA", "marketing_start_date": "20210917", "listing_expiration_date": "20261231"}