Package 50090-7182-0

Brand: varenicline

Generic: varenicline tartrate
NDC Package

Package Facts

Identity

Package NDC 50090-7182-0
Digits Only 5009071820
Product NDC 50090-7182
Description

56 TABLET, FILM COATED in 1 BOTTLE (50090-7182-0)

Marketing

Marketing Status
Marketed Since 2024-06-11
Brand varenicline
Generic varenicline tartrate
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "14f8492b-71a7-45a8-9268-a3b679d88248", "openfda": {"unii": ["82269ASB48"], "rxcui": ["636676"], "spl_set_id": ["6351047a-9896-4a30-8e49-4d306ce9c9c0"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "56 TABLET, FILM COATED in 1 BOTTLE (50090-7182-0)", "package_ndc": "50090-7182-0", "marketing_start_date": "20240611"}], "brand_name": "varenicline", "product_id": "50090-7182_14f8492b-71a7-45a8-9268-a3b679d88248", "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": "50090-7182", "generic_name": "varenicline tartrate", "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": "ANDA214557", "marketing_category": "ANDA", "marketing_start_date": "20230825", "listing_expiration_date": "20261231"}