NDC Code | 50436-3763-5 |
Package Description | 10 TABLET in 1 BOTTLE (50436-3763-5) |
Product NDC | 50436-3763 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Diphenoxylate Hydrochloride And Atropine Sulfate |
Non-Proprietary Name | Diphenoxylate Hydrochloride And Atropine Sulfate |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20130227 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Application Number | NDA012462 |
Manufacturer | Unit Dose Services |
Substance Name | DIPHENOXYLATE HYDROCHLORIDE; ATROPINE SULFATE |
Strength | 2.5; .025 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Antidiarrheal [EPC],Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA] |
DEA Schedule | CV |