nebivolol

Generic: nebivolol

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

Drug Facts

Product Profile

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

nebivolol hydrochloride 2.5 mg/1

Manufacturer
Novadoz Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 72205-150
Product ID 72205-150_e54ddb53-542b-4183-8950-5b3947ecead0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217397
Listing Expiration 2026-12-31
Marketing Start 2024-10-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72205150
Hyphenated Format 72205-150

Supplemental Identifiers

RxCUI
387013 751612 751618 827073
UPC
0372205150300 0372205150911 0372205152915 0372205152304 0372205150904 0372205153905 0372205153912 0372205153301 0372205151901 0372205151918 0372205151307 0372205152908
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 ANDA217397 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (72205-150-30)
  • 90 TABLET in 1 BOTTLE (72205-150-90)
  • 100 TABLET in 1 BOTTLE (72205-150-91)
  • 100 TABLET in 1 BOX, UNIT-DOSE (72205-150-99)
source: ndc

Packages (4)

72205-150-30 30 TABLET in 1 BOTTLE (72205-150-30) 72205-150-90 90 TABLET in 1 BOTTLE (72205-150-90) 72205-150-91 100 TABLET in 1 BOTTLE (72205-150-91) 72205-150-99 100 TABLET in 1 BOX, UNIT-DOSE (72205-150-99)

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": "e54ddb53-542b-4183-8950-5b3947ecead0", "openfda": {"upc": ["0372205150300", "0372205150911", "0372205152915", "0372205152304", "0372205150904", "0372205153905", "0372205153912", "0372205153301", "0372205151901", "0372205151918", "0372205151307", "0372205152908"], "unii": ["JGS34J7L9I"], "rxcui": ["387013", "751612", "751618", "827073"], "spl_set_id": ["e54ddb53-542b-4183-8950-5b3947ecead0"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72205-150-30)", "package_ndc": "72205-150-30", "marketing_start_date": "20241122"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72205-150-90)", "package_ndc": "72205-150-90", "marketing_start_date": "20241122"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (72205-150-91)", "package_ndc": "72205-150-91", "marketing_start_date": "20241122"}, {"sample": false, "description": "100 TABLET in 1 BOX, UNIT-DOSE (72205-150-99)", "package_ndc": "72205-150-99", "marketing_start_date": "20241122"}], "brand_name": "NEBIVOLOL", "product_id": "72205-150_e54ddb53-542b-4183-8950-5b3947ecead0", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72205-150", "generic_name": "NEBIVOLOL", "labeler_name": "Novadoz Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NEBIVOLOL", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA217397", "marketing_category": "ANDA", "marketing_start_date": "20241001", "listing_expiration_date": "20261231"}