Package 62559-490-01

{"route": ["ORAL"], "spl_id": "540ac802-a419-42f7-8f7f-d770ea165243", "openfda": {"upc": ["0362559490016"], "unii": ["03J5ZE7KA5", "W24OD7YW48"], "rxcui": ["1190572"], "spl_set_id": ["73dc5f91-d562-44c5-a556-66c96ed1dd82"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (62559-490-01)", "package_ndc": "62559-490-01", "marketing_start_date": "20170707"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (62559-490-10)", "package_ndc": "62559-490-10", "marketing_start_date": "20170707"}], "brand_name": "Diphenoxylate Hydrochloride and Atropine Sulfate", "product_id": "62559-490_540ac802-a419-42f7-8f7f-d770ea165243", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Antidiarrheal [EPC]", "Cholinergic Antagonists [MoA]", "Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "62559-490", "dea_schedule": "CV", "generic_name": "Diphenoxylate Hydrochloride and Atropine Sulfate", "labeler_name": "ANI Pharmaceuticals, Inc.", "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": "ANDA086727", "marketing_category": "ANDA", "marketing_start_date": "20170707", "listing_expiration_date": "20261231"}