Venlafaxine Hydrochloride 70710-1698
Product NDC
70710-1698- Manufacturer
- Zydus Pharmaceuticals Usa Inc.
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 18, 2023
- Listing Expires
- December 31, 2027
- Application
- ANDA090174
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Venlafaxine Hydrochloride | 37.5 mg/1 |
Drug Class
Norepinephrine Uptake Inhibitors [MoA]Serotonin Uptake Inhibitors [MoA]Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
Packaging Options(5)
1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70710-1698-0)
30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70710-1698-3)
10 BLISTER PACK in 1 CARTON (70710-1698-4) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70710-1698-2)
500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70710-1698-5)
90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70710-1698-9)