Package 68382-914-84

{"route": ["ORAL"], "spl_id": "e34fafdf-2fda-4031-9202-6d7e85925dc1", "openfda": {"unii": ["DA87705X9K"], "rxcui": ["603203", "603206", "603208"], "spl_set_id": ["c35e019d-ec34-4e61-9400-a7ae7913e025"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68382-914-06)", "package_ndc": "68382-914-06", "marketing_start_date": "20200430"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68382-914-16)", "package_ndc": "68382-914-16", "marketing_start_date": "20200430"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (68382-914-84)  / 10 TABLET in 1 BLISTER PACK (68382-914-30)", "package_ndc": "68382-914-84", "marketing_start_date": "20200430"}], "brand_name": "Erlotinib", "product_id": "68382-914_e34fafdf-2fda-4031-9202-6d7e85925dc1", "dosage_form": "TABLET", "pharm_class": ["Kinase Inhibitor [EPC]", "Protein Kinase Inhibitors [MoA]"], "product_ndc": "68382-914", "generic_name": "Erlotinib", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Erlotinib", "active_ingredients": [{"name": "ERLOTINIB HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA213065", "marketing_category": "ANDA", "marketing_start_date": "20200430", "listing_expiration_date": "20261231"}