Package 0904-7413-35
Brand: varenicline
Generic: varenicline tartratePackage Facts
Identity
Package NDC
0904-7413-35
Digits Only
0904741335
Product NDC
0904-7413
Description
56 TABLET, FILM COATED in 1 BOTTLE (0904-7413-35)
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": "1297c291-da28-4a73-9c28-d5adee36d7b7", "openfda": {"unii": ["82269ASB48"], "rxcui": ["636671", "636676", "749289"], "spl_set_id": ["1297c291-da28-4a73-9c28-d5adee36d7b7"], "manufacturer_name": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "56 TABLET, FILM COATED in 1 BOTTLE (0904-7413-35)", "package_ndc": "0904-7413-35", "marketing_start_date": "20231218"}], "brand_name": "varenicline", "product_id": "0904-7413_1297c291-da28-4a73-9c28-d5adee36d7b7", "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": "0904-7413", "generic_name": "varenicline tartrate", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "varenicline", "active_ingredients": [{"name": "VARENICLINE TARTRATE", "strength": ".5 mg/1"}], "application_number": "ANDA214557", "marketing_category": "ANDA", "marketing_start_date": "20231218", "listing_expiration_date": "20261231"}