Package 71921-309-56
Brand: varenicline tartrate
Generic: varenicline tartratePackage Facts
Identity
Package NDC
71921-309-56
Digits Only
7192130956
Product NDC
71921-309
Description
56 TABLET, FILM COATED in 1 BOTTLE (71921-309-56)
Marketing
Marketing Status
Brand
varenicline tartrate
Generic
varenicline tartrate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b9c8b1e-6193-4d8e-9b50-6aca27294263", "openfda": {"unii": ["82269ASB48"], "rxcui": ["636671", "636676", "749289"], "spl_set_id": ["2b9c8b1e-6193-4d8e-9b50-6aca27294263"], "manufacturer_name": ["Florida Pharmaceutical Products, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "56 TABLET, FILM COATED in 1 BOTTLE (71921-309-56)", "package_ndc": "71921-309-56", "marketing_start_date": "20241101"}], "brand_name": "Varenicline tartrate", "product_id": "71921-309_2b9c8b1e-6193-4d8e-9b50-6aca27294263", "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": "71921-309", "generic_name": "Varenicline tartrate", "labeler_name": "Florida Pharmaceutical Products, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Varenicline tartrate", "active_ingredients": [{"name": "VARENICLINE TARTRATE", "strength": "1 mg/1"}], "application_number": "ANDA219106", "marketing_category": "ANDA", "marketing_start_date": "20241101", "listing_expiration_date": "20261231"}