| NDC Code: |
59762-1061 |
| Proprietary Name: |
Diphenoxylate Hydrochloride and Atropine Sulfate |
| Suffix: |
|
| Non-Proprietary Name: |
DIPHENOXYLATE HYDROCHLORIDE and ATROPINE SULFATE |
| Dosage Form: |
TABLET |
| Method: |
ORAL |
| Original Marketing Date: |
27-02-2013 |
| Category Name: |
NDA AUTHORIZED GENERIC |
| Application Number: |
NDA012462 |
| Labeler: |
GREENSTONE LLC |
| Substance Name: |
ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE |
| Active Numerator Strength: |
.025; 2.5 |
| Active Ingredient Unit: |
mg/1; mg/1 |
| Pharm Classes: |
Antidiarrheal [EPC],Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA] |
| DEA Schedule: |
CV |
