Package 70710-1614-6

Brand: varenicline

Generic: varenicline
NDC Package

Package Facts

Identity

Package NDC 70710-1614-6
Digits Only 7071016146
Product NDC 70710-1614
Description

56 TABLET, FILM COATED in 1 BOTTLE (70710-1614-6)

Marketing

Marketing Status
Marketed Since 2023-06-13
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": "985b4791-e204-4342-9cab-052cccf4a730", "openfda": {"upc": ["0370710161361", "0370710161460"], "unii": ["82269ASB48"], "rxcui": ["636671", "636676"], "spl_set_id": ["1d4c9535-f185-4ea3-9140-60c4bb77f736"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "56 TABLET, FILM COATED in 1 BOTTLE (70710-1614-6)", "package_ndc": "70710-1614-6", "marketing_start_date": "20230613"}], "brand_name": "Varenicline", "product_id": "70710-1614_985b4791-e204-4342-9cab-052cccf4a730", "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": "70710-1614", "generic_name": "Varenicline", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Varenicline", "active_ingredients": [{"name": "VARENICLINE TARTRATE", "strength": "1 mg/1"}], "application_number": "ANDA216723", "marketing_category": "ANDA", "marketing_start_date": "20230613", "listing_expiration_date": "20261231"}