Venlafaxine Hydrochloride 68382-0036
Product NDC
68382-0036- Manufacturer
- Zydus Pharmaceuticals Usa Inc.
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 1, 2011
- Listing Expires
- December 31, 2026
- Application
- ANDA090174
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Venlafaxine Hydrochloride | 150 mg/1 |
Drug Class
Norepinephrine Uptake Inhibitors [MoA]Serotonin Uptake Inhibitors [MoA]Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
Packaging Options(3)
30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-036-06)
1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-036-10)
90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-036-16)