Package 60505-3613-5

Brand: varenicline

Generic: varenicline
NDC Package

Package Facts

Identity

Package NDC 60505-3613-5
Digits Only 6050536135
Product NDC 60505-3613
Description

56 TABLET, FILM COATED in 1 BOTTLE (60505-3613-5)

Marketing

Marketing Status
Marketed Since 2023-01-30
Brand varenicline
Generic varenicline
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4fb749d9-409f-d07a-7006-394063557043", "openfda": {"upc": ["0360505361458", "0360505361328"], "unii": ["82269ASB48"], "rxcui": ["636671", "636676", "749289", "749788"], "spl_set_id": ["78d1857f-8708-5410-792f-4a3e5e7971a5"], "manufacturer_name": ["Apotex Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "56 TABLET, FILM COATED in 1 BOTTLE (60505-3613-5)", "package_ndc": "60505-3613-5", "marketing_start_date": "20230130"}], "brand_name": "VARENICLINE", "product_id": "60505-3613_4fb749d9-409f-d07a-7006-394063557043", "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": "60505-3613", "generic_name": "VARENICLINE", "labeler_name": "Apotex Corp", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VARENICLINE", "active_ingredients": [{"name": "VARENICLINE TARTRATE", "strength": ".5 mg/1"}], "application_number": "ANDA201962", "marketing_category": "ANDA", "marketing_start_date": "20230130", "listing_expiration_date": "20261231"}