Package 72189-336-10

{"route": ["ORAL"], "spl_id": "2c3d9a97-2f79-1c66-e063-6294a90ab5c4", "openfda": {"unii": ["03J5ZE7KA5", "W24OD7YW48"], "rxcui": ["1190572"], "spl_set_id": ["d9a36478-4788-4107-e053-2a95a90ad6da"], "manufacturer_name": ["Direct Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (72189-336-10)", "package_ndc": "72189-336-10", "marketing_start_date": "20220307"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-336-30)", "package_ndc": "72189-336-30", "marketing_start_date": "20220307"}], "brand_name": "DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE", "product_id": "72189-336_2c3d9a97-2f79-1c66-e063-6294a90ab5c4", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Antidiarrheal [EPC]", "Cholinergic Antagonists [MoA]", "Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "72189-336", "dea_schedule": "CV", "generic_name": "DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE", "labeler_name": "Direct Rx", "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": "ANDA213413", "marketing_category": "ANDA", "marketing_start_date": "20220307", "listing_expiration_date": "20261231"}