Venlafaxine 65862-0408
Generic: Venlafaxine Hydrochloride
Product NDC
65862-0408- Manufacturer
- Aurobindo Pharma Limited
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 7, 2010
- Listing Expires
- December 31, 2026
- Application
- ANDA090555
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Venlafaxine Hydrochloride | 100 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 (65862-408-01)
10 BLISTER PACK in 1 CARTON (65862-408-10) / 10 TABLET in 1 BLISTER PACK
20 TABLET in 1 BOTTLE (65862-408-20)
6000 TABLET in 1 BOTTLE (65862-408-66)
90 TABLET in 1 BOTTLE (65862-408-90)
1000 TABLET in 1 BOTTLE (65862-408-99)