Package 68180-346-06
Brand: darunavir
Generic: darunavirPackage Facts
Identity
Package NDC
68180-346-06
Digits Only
6818034606
Product NDC
68180-346
Description
30 TABLET, FILM COATED in 1 BOTTLE (68180-346-06)
Marketing
Marketing Status
Brand
darunavir
Generic
darunavir
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f2b03ba0-704c-447a-a7ab-b4eb00243295", "openfda": {"upc": ["0368180345077", "0368180346067"], "unii": ["33O78XF0BW"], "rxcui": ["670026", "1359269"], "spl_set_id": ["56daf67e-7501-4cd5-be22-566d7997d42e"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68180-346-06)", "package_ndc": "68180-346-06", "marketing_start_date": "20230601"}], "brand_name": "DARUNAVIR", "product_id": "68180-346_f2b03ba0-704c-447a-a7ab-b4eb00243295", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Cytochrome P450 3A Inhibitors [MoA]", "HIV Protease Inhibitors [MoA]", "Protease Inhibitor [EPC]"], "product_ndc": "68180-346", "generic_name": "DARUNAVIR", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DARUNAVIR", "active_ingredients": [{"name": "DARUNAVIR ETHANOLATE", "strength": "800 mg/1"}], "application_number": "ANDA202073", "marketing_category": "ANDA", "marketing_start_date": "20230601", "listing_expiration_date": "20261231"}