Package 69315-910-10
Brand: diphenoxylate hydrochloride and atropine sulfate
Generic: diphenoxylate hydrochloride and atropine sulfatePackage Facts
Identity
Package NDC
69315-910-10
Digits Only
6931591010
Product NDC
69315-910
Description
1000 TABLET in 1 BOTTLE (69315-910-10)
Marketing
Marketing Status
Brand
diphenoxylate hydrochloride and atropine sulfate
Generic
diphenoxylate hydrochloride and atropine sulfate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "af054a1c-a0a1-4097-8170-3e7b070ad830", "openfda": {"upc": ["0369315910092", "0369315910016", "0369315910108"], "unii": ["03J5ZE7KA5", "W24OD7YW48"], "rxcui": ["1190572"], "spl_set_id": ["1c188bc9-7c21-4717-94a0-cdfb581fb776"], "manufacturer_name": ["Leading Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69315-910-01)", "package_ndc": "69315-910-01", "marketing_start_date": "20200315"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (69315-910-09)", "package_ndc": "69315-910-09", "marketing_start_date": "20200315"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (69315-910-10)", "package_ndc": "69315-910-10", "marketing_start_date": "20200315"}], "brand_name": "Diphenoxylate Hydrochloride and Atropine Sulfate", "product_id": "69315-910_af054a1c-a0a1-4097-8170-3e7b070ad830", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Antidiarrheal [EPC]", "Cholinergic Antagonists [MoA]", "Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "69315-910", "dea_schedule": "CV", "generic_name": "diphenoxylate hydrochloride and atropine sulfate", "labeler_name": "Leading Pharma, 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": "ANDA213413", "marketing_category": "ANDA", "marketing_start_date": "20200315", "listing_expiration_date": "20261231"}