Package 43598-908-56
Brand: varenicline tartrate
Generic: varenicline tartratePackage Facts
Identity
Package NDC
43598-908-56
Digits Only
4359890856
Product NDC
43598-908
Description
56 TABLET, FILM COATED in 1 BOTTLE (43598-908-56)
Marketing
Marketing Status
Brand
varenicline tartrate
Generic
varenicline tartrate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "65233c50-9a25-15c3-cc2b-98713a8173b2", "openfda": {"unii": ["82269ASB48"], "rxcui": ["636671", "636676", "749289", "749788"], "spl_set_id": ["16ee0a83-88d7-97de-1e07-f9e6dcb5c934"], "manufacturer_name": ["Dr. Reddys Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "56 TABLET, FILM COATED in 1 BOTTLE (43598-908-56)", "package_ndc": "43598-908-56", "marketing_start_date": "20241213"}], "brand_name": "varenicline tartrate", "product_id": "43598-908_65233c50-9a25-15c3-cc2b-98713a8173b2", "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": "43598-908", "generic_name": "varenicline tartrate", "labeler_name": "Dr. Reddys Laboratories Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "varenicline tartrate", "active_ingredients": [{"name": "VARENICLINE TARTRATE", "strength": "1 mg/1"}], "application_number": "ANDA215931", "marketing_category": "ANDA", "marketing_start_date": "20241213", "listing_expiration_date": "20261231"}