Venlafaxine 70771-1652
Product NDC
70771-1652- Manufacturer
- Zydus Lifesciences Limited
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 1, 2022
- Listing Expires
- December 31, 2026
- Application
- ANDA215622
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Venlafaxine Hydrochloride | 225 mg/1 |
Drug Class
Norepinephrine Uptake Inhibitors [MoA]Serotonin Uptake Inhibitors [MoA]Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
Packaging Options(3)
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1652-1)
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1652-3)
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1652-9)