| NDC Code | 55111-546-01 |
|---|
| Package Description | 100 TABLET in 1 BOTTLE (55111-546-01) |
|---|
| Product NDC | 55111-546 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Venlafaxine Hydrochloride |
|---|
| Non-Proprietary Name | Venlafaxine Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20080616 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA078301 |
|---|
| Manufacturer | Dr. Reddy's Laboratories Limited |
|---|
| Substance Name | VENLAFAXINE HYDROCHLORIDE |
|---|
| Strength | 37.5 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC] |
|---|