Venlafaxine Hydrochloride 31722-0004
Product NDC
31722-0004- Manufacturer
- Camber Pharmaceuticals, Inc.
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 8, 2019
- Listing Expires
- December 31, 2026
- Application
- ANDA212277
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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)
10 BLISTER PACK in 1 CARTON (31722-004-01) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK
500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-004-05)
30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-004-30)
90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-004-90)