| NDC Code | 51079-482-20 |
|---|
| Package Description | 100 BLISTER PACK in 1 CARTON (51079-482-20) > 1 TABLET in 1 BLISTER PACK (51079-482-01) |
|---|
| Product NDC | 51079-482 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Venlafaxine Hydrochloride |
|---|
| Non-Proprietary Name | Venlafaxine Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20080715 |
|---|
| End Marketing Date | 20201231 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA077166 |
|---|
| Manufacturer | Mylan Institutional Inc. |
|---|
| Substance Name | VENLAFAXINE HYDROCHLORIDE |
|---|
| Strength | 75 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
|---|