Package 68462-864-01

{"route": ["ORAL"], "spl_id": "440a4208-83cc-4ffa-952c-d9c0745c342a", "openfda": {"upc": ["0368462862018", "0368462864012", "0368462863015", "0368462861011"], "unii": ["9WP59609J6"], "rxcui": ["991039", "991044", "991188", "991194", "991336"], "spl_set_id": ["a6065ac5-a111-449b-b51b-8bc2907d1ddb"], "manufacturer_name": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68462-864-01)", "package_ndc": "68462-864-01", "marketing_start_date": "20210323"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (68462-864-10)", "package_ndc": "68462-864-10", "marketing_start_date": "20210323"}], "brand_name": "Chlorpromazine Hydrochloride", "product_id": "68462-864_440a4208-83cc-4ffa-952c-d9c0745c342a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "68462-864", "generic_name": "Chlorpromazine Hydrochloride", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorpromazine Hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA212144", "marketing_category": "ANDA", "marketing_start_date": "20210323", "listing_expiration_date": "20261231"}