Venlafaxine Hydrochloride 43598-0999
Product NDC
43598-0999- Manufacturer
- Dr.reddys Laboratories Inc
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 9, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA078421
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 | 37.5 mg/1 |
Drug Class
Norepinephrine Uptake Inhibitors [MoA]Serotonin Uptake Inhibitors [MoA]Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
Packaging Options(3)
1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43598-999-10)
30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43598-999-30)
90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43598-999-90)