| NDC Code | 60429-866-90 |
|---|
| Package Description | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (60429-866-90) |
|---|
| Product NDC | 60429-866 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Venlafaxine Hydrochloride |
|---|
| Non-Proprietary Name | Venlafaxine Hydrochloride |
|---|
| Dosage Form | TABLET, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20170324 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA205468 |
|---|
| Manufacturer | Golden State Medical Supply |
|---|
| Substance Name | VENLAFAXINE HYDROCHLORIDE |
|---|
| Strength | 150 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC] |
|---|