| NDC Code | 75834-218-00 |
|---|
| Package Description | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (75834-218-00) |
|---|
| Product NDC | 75834-218 |
|---|
| 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 | 20190906 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA211323 |
|---|
| Manufacturer | Nivagen Pharmaceuticals, Inc. |
|---|
| 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] |
|---|