Venlafaxine Hydrochloride 43598-0002
Product NDC
43598-0002- 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
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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)
500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43598-002-05)
30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43598-002-30)
90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43598-002-90)