Package 60505-3615-4

Brand: varenicline

Generic: varenicline
NDC Package

Package Facts

Identity

Package NDC 60505-3615-4
Digits Only 6050536154
Product NDC 60505-3615
Description

1 KIT in 1 CARTON (60505-3615-4) * 11 TABLET, FILM COATED in 1 BLISTER PACK (60505-3606-1) * 42 TABLET, FILM COATED in 1 BLISTER PACK (60505-3607-1)

Marketing

Marketing Status
Marketed Since 2024-01-15
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": "1 KIT in 1 CARTON (60505-3615-4)  *  11 TABLET, FILM COATED in 1 BLISTER PACK (60505-3606-1)  *  42 TABLET, FILM COATED in 1 BLISTER PACK (60505-3607-1)", "package_ndc": "60505-3615-4", "marketing_start_date": "20240115"}], "brand_name": "VARENICLINE", "product_id": "60505-3615_4fb749d9-409f-d07a-7006-394063557043", "dosage_form": "KIT", "product_ndc": "60505-3615", "generic_name": "VARENICLINE", "labeler_name": "Apotex Corp", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VARENICLINE", "application_number": "ANDA201962", "marketing_category": "ANDA", "marketing_start_date": "20240115", "listing_expiration_date": "20261231"}