Package 31722-678-56
Brand: varenicline
Generic: varenicline tartratePackage Facts
Identity
Package NDC
31722-678-56
Digits Only
3172267856
Product NDC
31722-678
Description
56 TABLET, FILM COATED in 1 BOTTLE (31722-678-56)
Marketing
Marketing Status
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": "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": "56 TABLET, FILM COATED in 1 BOTTLE (31722-678-56)", "package_ndc": "31722-678-56", "marketing_start_date": "20231023"}], "brand_name": "Varenicline", "product_id": "31722-678_09a2708f-ed1b-b986-e063-6394a90a8fb5", "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": "31722-678", "generic_name": "Varenicline tartrate", "labeler_name": "Camber Pharmaceuticals, Inc.", "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": "20231023", "listing_expiration_date": "20261231"}