Venlafaxine Hydrochloride 68788-8774
Product NDC
68788-8774- Manufacturer
- Preferred Pharmaceuticals Inc.
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 20, 2024
- Listing Expires
- December 31, 2027
- 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(6)
100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8774-1)
20 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8774-2)
30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8774-3)
60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8774-6)
120 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8774-8)
90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8774-9)