Package 0406-1236-01

{"route": ["ORAL"], "spl_id": "c7a8d21f-365e-4a00-a7bf-4ee5fc6c2406", "openfda": {"upc": ["0304061236102"], "unii": ["03J5ZE7KA5", "W24OD7YW48"], "rxcui": ["1190572"], "spl_set_id": ["24915aa0-1600-44bb-99fc-46529a794124"], "manufacturer_name": ["SpecGx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0406-1236-01)", "package_ndc": "0406-1236-01", "marketing_start_date": "20201030"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (0406-1236-10)", "package_ndc": "0406-1236-10", "marketing_start_date": "20201030"}], "brand_name": "Diphenoxylate Hydrochloride and Atropine Sulfate", "product_id": "0406-1236_c7a8d21f-365e-4a00-a7bf-4ee5fc6c2406", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Antidiarrheal [EPC]", "Cholinergic Antagonists [MoA]", "Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "0406-1236", "dea_schedule": "CV", "generic_name": "diphenoxylate hydrochloride and atropine sulfate", "labeler_name": "SpecGx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diphenoxylate Hydrochloride and Atropine Sulfate", "active_ingredients": [{"name": "ATROPINE SULFATE", "strength": ".025 mg/1"}, {"name": "DIPHENOXYLATE HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA213335", "marketing_category": "ANDA", "marketing_start_date": "20201030", "listing_expiration_date": "20261231"}