Venlafaxine Hydrochloride 10135-0827
Product NDC
10135-0827- Manufacturer
- Marlex Pharmaceuticals, Inc.
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 1, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA201272
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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(4)
1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (10135-827-10)
30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (10135-827-30)
15 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (10135-827-75)
90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (10135-827-90)