Package 70954-158-20

{"route": ["ORAL"], "spl_id": "d4edcb5d-dbe9-44c4-a0a9-d3b6aba4c22d", "openfda": {"unii": ["63FN7G03XY"], "rxcui": ["197464", "197465", "197466"], "spl_set_id": ["a4b80e69-b7c7-471a-8ce8-4e992808c669"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70954-158-10)", "package_ndc": "70954-158-10", "marketing_start_date": "20220616"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (70954-158-20)", "package_ndc": "70954-158-20", "marketing_start_date": "20220701"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (70954-158-30)", "package_ndc": "70954-158-30", "marketing_start_date": "20230821"}, {"sample": false, "description": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (70954-158-50)  / 1 TABLET in 1 BLISTER PACK (70954-158-40)", "package_ndc": "70954-158-50", "marketing_start_date": "20250615"}], "brand_name": "Clorazepate Dipotassium", "product_id": "70954-158_d4edcb5d-dbe9-44c4-a0a9-d3b6aba4c22d", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "70954-158", "dea_schedule": "CIV", "generic_name": "Clorazepate Dipotassium", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clorazepate Dipotassium", "active_ingredients": [{"name": "CLORAZEPATE DIPOTASSIUM", "strength": "7.5 mg/1"}], "application_number": "ANDA213730", "marketing_category": "ANDA", "marketing_start_date": "20220616", "listing_expiration_date": "20261231"}