nebivolol

Generic: nebivolol

Labeler: lifestar pharma llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nebivolol
Generic Name nebivolol
Labeler lifestar pharma llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

nebivolol hydrochloride 20 mg/1

Manufacturer
Lifestar Pharma LLC

Identifiers & Regulatory

Product NDC 70756-293
Product ID 70756-293_2ffb359c-7e4b-44ef-a0c7-451ac966f6b6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216172
Listing Expiration 2026-12-31
Marketing Start 2022-11-14

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70756293
Hyphenated Format 70756-293

Supplemental Identifiers

RxCUI
387013 751612 751618 827073
UPC
0370756291305 0370756291909 0370756025306 0370756292906 0370756293903
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 ANDA216172 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (70756-293-30)
  • 90 TABLET in 1 BOTTLE (70756-293-90)
source: ndc

Packages (2)

70756-293-30 30 TABLET in 1 BOTTLE (70756-293-30) 70756-293-90 90 TABLET in 1 BOTTLE (70756-293-90)

Ingredients (1)

nebivolol hydrochloride (20 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": "2ffb359c-7e4b-44ef-a0c7-451ac966f6b6", "openfda": {"upc": ["0370756291305", "0370756291909", "0370756025306", "0370756292906", "0370756293903"], "unii": ["JGS34J7L9I"], "rxcui": ["387013", "751612", "751618", "827073"], "spl_set_id": ["2639abce-a5ca-4b7f-99d7-026ab3233aaa"], "manufacturer_name": ["Lifestar Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (70756-293-30)", "package_ndc": "70756-293-30", "marketing_start_date": "20221114"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (70756-293-90)", "package_ndc": "70756-293-90", "marketing_start_date": "20221114"}], "brand_name": "Nebivolol", "product_id": "70756-293_2ffb359c-7e4b-44ef-a0c7-451ac966f6b6", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70756-293", "generic_name": "Nebivolol", "labeler_name": "Lifestar Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nebivolol", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA216172", "marketing_category": "ANDA", "marketing_start_date": "20221114", "listing_expiration_date": "20261231"}