Venlafaxine Hydrochloride 70518-2259
Product NDC
70518-2259- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 9, 2019
- Listing Expires
- December 31, 2027
- Application
- ANDA200834
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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)
90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2259-1)
30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70518-2259-2)
30 POUCH in 1 BOX (70518-2259-5) / 1 CAPSULE, EXTENDED RELEASE in 1 POUCH (70518-2259-6)