Package 72162-2218-2

Brand: varenicline

Generic: varenicline
NDC Package

Package Facts

Identity

Package NDC 72162-2218-2
Digits Only 7216222182
Product NDC 72162-2218
Description

56 TABLET, FILM COATED in 1 BOTTLE (72162-2218-2)

Marketing

Marketing Status
Marketed Since 2023-01-30
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": "e3cc710d-23d8-4d68-b854-b6f5f4e737fc", "openfda": {"unii": ["82269ASB48"], "rxcui": ["636671"], "spl_set_id": ["e3cc710d-23d8-4d68-b854-b6f5f4e737fc"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "56 TABLET, FILM COATED in 1 BOTTLE (72162-2218-2)", "package_ndc": "72162-2218-2", "marketing_start_date": "20230130"}], "brand_name": "VARENICLINE", "product_id": "72162-2218_e3cc710d-23d8-4d68-b854-b6f5f4e737fc", "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": "72162-2218", "generic_name": "VARENICLINE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VARENICLINE", "active_ingredients": [{"name": "VARENICLINE TARTRATE", "strength": ".5 mg/1"}], "application_number": "ANDA201962", "marketing_category": "ANDA", "marketing_start_date": "20230130", "listing_expiration_date": "20261231"}