nebivolol

Generic: nebivolol

Labeler: modavar pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nebivolol
Generic Name nebivolol
Labeler modavar pharmaceuticals llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

nebivolol hydrochloride 2.5 mg/1

Manufacturer
Modavar Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 72241-032
Product ID 72241-032_53d2f49b-b0b8-46fc-b80d-1ac3756e7e7c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208717
Listing Expiration 2026-12-31
Marketing Start 2017-12-29

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72241032
Hyphenated Format 72241-032

Supplemental Identifiers

RxCUI
387013 751612 751618 827073
UPC
0372241032110 0372241034053 0372241034220 0372241033223 0372241035227 0372241033117
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 ANDA208717 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (72241-032-04)
  • 100 TABLET in 1 BOTTLE (72241-032-05)
  • 1000 TABLET in 1 BOTTLE (72241-032-11)
  • 30 TABLET in 1 BOTTLE (72241-032-22)
source: ndc

Packages (4)

72241-032-04 90 TABLET in 1 BOTTLE (72241-032-04) 72241-032-05 100 TABLET in 1 BOTTLE (72241-032-05) 72241-032-11 1000 TABLET in 1 BOTTLE (72241-032-11) 72241-032-22 30 TABLET in 1 BOTTLE (72241-032-22)

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": "53d2f49b-b0b8-46fc-b80d-1ac3756e7e7c", "openfda": {"upc": ["0372241032110", "0372241034053", "0372241034220", "0372241033223", "0372241035227", "0372241033117"], "unii": ["JGS34J7L9I"], "rxcui": ["387013", "751612", "751618", "827073"], "spl_set_id": ["19d20396-ade8-400e-94f4-69913637d051"], "manufacturer_name": ["Modavar Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (72241-032-04)", "package_ndc": "72241-032-04", "marketing_start_date": "20211218"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (72241-032-05)", "package_ndc": "72241-032-05", "marketing_start_date": "20211218"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (72241-032-11)", "package_ndc": "72241-032-11", "marketing_start_date": "20211218"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (72241-032-22)", "package_ndc": "72241-032-22", "marketing_start_date": "20211218"}], "brand_name": "Nebivolol", "product_id": "72241-032_53d2f49b-b0b8-46fc-b80d-1ac3756e7e7c", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72241-032", "generic_name": "Nebivolol", "labeler_name": "Modavar Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nebivolol", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA208717", "marketing_category": "ANDA", "marketing_start_date": "20171229", "listing_expiration_date": "20261231"}