| NDC Code | 69367-417-30 |
|---|
| Package Description | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-417-30) |
|---|
| Product NDC | 69367-417 |
|---|
| 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 | 20251118 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA205468 |
|---|
| Manufacturer | Westminster Pharmaceuticals, LLC |
|---|
| 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] |
|---|