| NDC Code | 49884-771-01 |
|---|
| Package Description | 100 TABLET in 1 BOTTLE (49884-771-01) |
|---|
| Product NDC | 49884-771 |
|---|
| 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 | 20000526 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA040357 |
|---|
| Manufacturer | Par Pharmaceutical, 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 |
|---|