NDC Code | 68788-9135-7 |
Package Description | 21 TABLET in 1 BOTTLE, PLASTIC (68788-9135-7) |
Product NDC | 68788-9135 |
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 | 19771117 |
Marketing Category Name | ANDA |
Application Number | ANDA085762 |
Manufacturer | Preferred Pharmaceuticals, Inc. |
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 |