NDC Code | 54569-0222-1 |
Package Description | 20 TABLET in 1 BOTTLE, PLASTIC (54569-0222-1) |
Product NDC | 54569-0222 |
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 | 20101130 |
Marketing Category Name | ANDA |
Application Number | ANDA085762 |
Manufacturer | A-S Medication Solutions LLC |
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 |