Package 68071-4063-3
Brand: diphenoxylate hydrochloride and atropine sulfate
Generic: diphenoxylate hydrochloride and atropine sulfatePackage Facts
Identity
Package NDC
68071-4063-3
Digits Only
6807140633
Product NDC
68071-4063
Description
30 TABLET in 1 BOTTLE (68071-4063-3)
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": "1d8dd9e3-f2b7-7894-e063-6394a90a29d3", "openfda": {"upc": ["0368071406313"], "unii": ["03J5ZE7KA5", "W24OD7YW48"], "rxcui": ["1190572"], "spl_set_id": ["575c38b4-7ec0-6d25-e053-2a91aa0a80fc"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (68071-4063-1)", "package_ndc": "68071-4063-1", "marketing_start_date": "20170822"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (68071-4063-2)", "package_ndc": "68071-4063-2", "marketing_start_date": "20170822"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-4063-3)", "package_ndc": "68071-4063-3", "marketing_start_date": "20170822"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (68071-4063-5)", "package_ndc": "68071-4063-5", "marketing_start_date": "20170822"}], "brand_name": "Diphenoxylate Hydrochloride and Atropine Sulfate", "product_id": "68071-4063_1d8dd9e3-f2b7-7894-e063-6394a90a29d3", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Antidiarrheal [EPC]", "Cholinergic Antagonists [MoA]", "Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "68071-4063", "dea_schedule": "CV", "generic_name": "Diphenoxylate Hydrochloride and Atropine Sulfate", "labeler_name": "NuCare 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": "20170620", "listing_expiration_date": "20261231"}