Package 31722-690-31

Brand: varenicline

Generic: varenicline tartrate
NDC Package

Package Facts

Identity

Package NDC 31722-690-31
Digits Only 3172269031
Product NDC 31722-690
Description

1 KIT in 1 CARTON (31722-690-31) * 11 TABLET, FILM COATED in 1 BLISTER PACK * 42 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2023-10-23
Brand varenicline
Generic varenicline tartrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"spl_id": "09a2708f-ed1b-b986-e063-6394a90a8fb5", "openfda": {"upc": ["0331722678568", "0331722679565"], "unii": ["82269ASB48"], "rxcui": ["636671", "636676", "749289", "749788"], "spl_set_id": ["7bd1abc8-2689-496b-b3f2-1cefe218ff5a"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (31722-690-31)  *  11 TABLET, FILM COATED in 1 BLISTER PACK *  42 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "31722-690-31", "marketing_start_date": "20231023"}], "brand_name": "Varenicline", "product_id": "31722-690_09a2708f-ed1b-b986-e063-6394a90a8fb5", "dosage_form": "KIT", "product_ndc": "31722-690", "generic_name": "Varenicline tartrate", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Varenicline", "application_number": "ANDA214571", "marketing_category": "ANDA", "marketing_start_date": "20231023", "listing_expiration_date": "20261231"}