Package 50090-6446-0
Brand: varenicline
Generic: vareniclinePackage Facts
Identity
Package NDC
50090-6446-0
Digits Only
5009064460
Product NDC
50090-6446
Description
56 TABLET, FILM COATED in 1 BOTTLE (50090-6446-0)
Marketing
Marketing Status
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": "6fd1d19f-3d72-4c29-b97b-d5a11dbeeb0b", "openfda": {"unii": ["82269ASB48"], "rxcui": ["636676"], "spl_set_id": ["92bc4c24-6c4f-4acf-b747-e3ef0cab1297"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "56 TABLET, FILM COATED in 1 BOTTLE (50090-6446-0)", "package_ndc": "50090-6446-0", "marketing_start_date": "20230420"}], "brand_name": "VARENICLINE", "product_id": "50090-6446_6fd1d19f-3d72-4c29-b97b-d5a11dbeeb0b", "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": "50090-6446", "generic_name": "VARENICLINE", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VARENICLINE", "active_ingredients": [{"name": "VARENICLINE TARTRATE", "strength": "1 mg/1"}], "application_number": "ANDA201962", "marketing_category": "ANDA", "marketing_start_date": "20230126", "listing_expiration_date": "20261231"}