Venlafaxine Hydrochloride 65841-0671
Product NDC
65841-0671- Manufacturer
- Zydus Lifesciences Limited
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 13, 2008
- Listing Expires
- December 31, 2026
- Application
- ANDA077653
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Venlafaxine Hydrochloride | 25 mg/1 |
Drug Class
Norepinephrine Uptake Inhibitors [MoA]Serotonin Uptake Inhibitors [MoA]Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
Packaging Options(6)
100 TABLET in 1 BOTTLE (65841-671-01)
500 TABLET in 1 BOTTLE (65841-671-05)
30 TABLET in 1 BOTTLE (65841-671-06)
1000 TABLET in 1 BOTTLE (65841-671-10)
60 TABLET in 1 BOTTLE (65841-671-14)
90 TABLET in 1 BOTTLE (65841-671-16)