Venlafaxine Hydrochloride 00093-7384
Product NDC
00093-7384- Manufacturer
- Teva Pharmaceuticals Usa, Inc.
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 1, 2010
- Listing Expires
- December 31, 2027
- Application
- ANDA076565
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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(3)
500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-7384-05)
30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-7384-56)
90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-7384-98)