Venlafaxine Hydrochloride 75834-0217
Product NDC
75834-0217- Manufacturer
- Nivagen Pharmaceuticals, Inc.
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 6, 2019
- Listing Expires
- December 31, 2026
- Application
- ANDA211323
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Venlafaxine Hydrochloride | 75 mg/1 |
Drug Class
Norepinephrine Uptake Inhibitors [MoA]Serotonin Uptake Inhibitors [MoA]Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
Packaging Options(3)
1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (75834-217-00)
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (75834-217-30)
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (75834-217-90)