Package 70771-1510-4

{"route": ["ORAL"], "spl_id": "bea6994f-8f72-4c2d-8ba3-c74b10f8412d", "openfda": {"upc": ["0370771150618", "0370771150816", "0370771151011", "0370771150915"], "unii": ["9WP59609J6"], "rxcui": ["991039", "991044", "991188", "991194", "991336"], "spl_set_id": ["0ea5e0c6-0062-4be3-96f2-62397da3e77d"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": true, "description": "100 TABLET, FILM COATED in 1 BOTTLE (70771-1510-1)", "package_ndc": "70771-1510-1", "marketing_start_date": "20200127"}, {"sample": true, "description": "10 BLISTER PACK in 1 CARTON (70771-1510-4)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1510-2)", "package_ndc": "70771-1510-4", "marketing_start_date": "20200127"}], "brand_name": "Chlorpromazine hydrochloride", "product_id": "70771-1510_bea6994f-8f72-4c2d-8ba3-c74b10f8412d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70771-1510", "generic_name": "Chlorpromazine hydrochloride", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorpromazine hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA213368", "marketing_category": "ANDA", "marketing_start_date": "20200127", "listing_expiration_date": "20261231"}