Package 70748-127-49
Brand: varenicline
Generic: vareniclinePackage Facts
Identity
Package NDC
70748-127-49
Digits Only
7074812749
Product NDC
70748-127
Description
56 TABLET, FILM COATED in 1 BOTTLE (70748-127-49)
Marketing
Marketing Status
Brand
varenicline
Generic
varenicline
Sample Package
Yes
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3647a217-0da1-4778-adea-08d19a9c446f", "openfda": {"upc": ["0370748128497", "0370748127490"], "unii": ["82269ASB48"], "rxcui": ["636671", "636676", "749289"], "spl_set_id": ["bf20c4cc-1731-4873-8de1-b93d17591e9f"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": true, "description": "56 TABLET, FILM COATED in 1 BOTTLE (70748-127-49)", "package_ndc": "70748-127-49", "marketing_start_date": "20240109"}], "brand_name": "VARENICLINE", "product_id": "70748-127_3647a217-0da1-4778-adea-08d19a9c446f", "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": "70748-127", "generic_name": "VARENICLINE", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VARENICLINE", "active_ingredients": [{"name": "VARENICLINE TARTRATE", "strength": ".5 mg/1"}], "application_number": "ANDA211862", "marketing_category": "ANDA", "marketing_start_date": "20240109", "listing_expiration_date": "20261231"}