Package 72603-873-01

Brand: nebivolol

Generic: nebivolol
NDC Package

Package Facts

Identity

Package NDC 72603-873-01
Digits Only 7260387301
Product NDC 72603-873
Product ID 72603-873_9a81733f-abb2-4090-a1e1-cbca356821e8
Description

30 TABLET in 1 BOTTLE (72603-873-01)

Marketing

Marketing Status
Marketed Since 2025-07-14
Brand nebivolol
Generic nebivolol
Sample Package No

Linked Drug Pages (1)

Nebivolol ndc-match (0.95)

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 (72603-873-01)", "package_ndc": "72603-873-01", "marketing_start_date": "20250714"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72603-873-02)", "package_ndc": "72603-873-02", "marketing_start_date": "20250714"}], "brand_name": "Nebivolol", "product_id": "72603-873_9a81733f-abb2-4090-a1e1-cbca356821e8", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72603-873", "generic_name": "Nebivolol", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nebivolol", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA212661", "marketing_category": "ANDA", "marketing_start_date": "20250714", "listing_expiration_date": "20261231"}