nebivolol

Generic: nebivolol

Labeler: northstar rxllc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nebivolol
Generic Name nebivolol
Labeler northstar rxllc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

nebivolol hydrochloride 5 mg/1

Manufacturer
NorthStar RxLLC

Identifiers & Regulatory

Product NDC 72603-871
Product ID 72603-871_9a81733f-abb2-4090-a1e1-cbca356821e8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212661
Listing Expiration 2026-12-31
Marketing Start 2025-07-14

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72603871
Hyphenated Format 72603-871

Supplemental Identifiers

RxCUI
387013 751612 751618 827073
UPC
0372603870015 0372603871029 0372603873023 0372603872019 0372603873016 0372603871012 0372603872026
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 ANDA212661 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (72603-871-01)
  • 90 TABLET in 1 BOTTLE (72603-871-02)
source: ndc

Packages (2)

72603-871-01 30 TABLET in 1 BOTTLE (72603-871-01) 72603-871-02 90 TABLET in 1 BOTTLE (72603-871-02)

Ingredients (1)

nebivolol hydrochloride (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": "9a81733f-abb2-4090-a1e1-cbca356821e8", "openfda": {"upc": ["0372603870015", "0372603871029", "0372603873023", "0372603872019", "0372603873016", "0372603871012", "0372603872026"], "unii": ["JGS34J7L9I"], "rxcui": ["387013", "751612", "751618", "827073"], "spl_set_id": ["9a81733f-abb2-4090-a1e1-cbca356821e8"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72603-871-01)", "package_ndc": "72603-871-01", "marketing_start_date": "20250714"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72603-871-02)", "package_ndc": "72603-871-02", "marketing_start_date": "20250714"}], "brand_name": "Nebivolol", "product_id": "72603-871_9a81733f-abb2-4090-a1e1-cbca356821e8", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72603-871", "generic_name": "Nebivolol", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nebivolol", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA212661", "marketing_category": "ANDA", "marketing_start_date": "20250714", "listing_expiration_date": "20261231"}