Package 72603-476-01

Brand: varenicline

Generic: varenicline tartrate
NDC Package

Package Facts

Identity

Package NDC 72603-476-01
Digits Only 7260347601
Product NDC 72603-476
Description

56 TABLET, FILM COATED in 1 BOTTLE (72603-476-01)

Marketing

Marketing Status
Marketed Since 2024-09-23
Brand varenicline
Generic varenicline tartrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2318a1aa-9c4c-5925-e063-6394a90a5222", "openfda": {"upc": ["0372603476019", "0372603477016"], "unii": ["82269ASB48"], "rxcui": ["636671", "636676", "749289"], "spl_set_id": ["9031aa0d-2f68-4b9d-903f-ac0e95cbf35f"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "56 TABLET, FILM COATED in 1 BOTTLE (72603-476-01)", "package_ndc": "72603-476-01", "marketing_start_date": "20240923"}], "brand_name": "Varenicline", "product_id": "72603-476_2318a1aa-9c4c-5925-e063-6394a90a5222", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinergic Agonists [MoA]", "Cholinergic Receptor Agonist [EPC]", "Partial Cholinergic Nicotinic Agonist [EPC]", "Partial Cholinergic Nicotinic Agonists [MoA]"], "product_ndc": "72603-476", "generic_name": "Varenicline tartrate", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Varenicline", "active_ingredients": [{"name": "VARENICLINE TARTRATE", "strength": ".5 mg/1"}], "application_number": "ANDA214571", "marketing_category": "ANDA", "marketing_start_date": "20240923", "listing_expiration_date": "20261231"}