Package 62135-618-12

{"route": ["ORAL"], "spl_id": "459bb891-bb8e-c6b4-e063-6294a90a676a", "openfda": {"upc": ["0362135618124"], "unii": ["03J5ZE7KA5", "W24OD7YW48"], "rxcui": ["1190572"], "spl_set_id": ["240b537e-ff9b-45e3-9398-584372bd707a"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE (62135-618-12)", "package_ndc": "62135-618-12", "marketing_start_date": "20220608"}], "brand_name": "Diphenoxylate hydrochloride and atropine sulfate", "product_id": "62135-618_459bb891-bb8e-c6b4-e063-6294a90a676a", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Antidiarrheal [EPC]", "Cholinergic Antagonists [MoA]", "Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "62135-618", "dea_schedule": "CV", "generic_name": "Diphenoxylate hydrochloride and atropine sulfate", "labeler_name": "Chartwell RX, 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": "ANDA207128", "marketing_category": "ANDA", "marketing_start_date": "20201021", "listing_expiration_date": "20261231"}