Venlafaxine Hydrochloride 71785-1008
Product NDC
71785-1008- Manufacturer
- Annora Pharma Private Limited
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 8, 2019
- Listing Expires
- December 31, 2026
- Application
- ANDA212277
Need to source Venlafaxine Hydrochloride? Find it on a pharmacy-to-pharmacy marketplace at better prices.
✓ DSCSA Compliant. ✓ Verified Pharmacies Only.P2P pharmacy marketplace.
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)
30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71785-1008-0)
90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71785-1008-1)
500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71785-1008-2)
10 BLISTER PACK in 1 CARTON (71785-1008-3) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK