Venlafaxine 57664-0393
Product NDC
57664-0393- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 13, 2008
- Listing Expires
- December 31, 2027
- Application
- ANDA078627
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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(1)
100 TABLET in 1 BOTTLE (57664-393-88)