Venlafaxine 72241-0077
Product NDC
72241-0077- Manufacturer
- Modavar Pharmaceuticals Llc
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 5, 2018
- Listing Expires
- December 31, 2026
- Application
- ANDA211323
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Venlafaxine Hydrochloride | 225 mg/1 |
Drug Class
Norepinephrine Uptake Inhibitors [MoA]Serotonin Uptake Inhibitors [MoA]Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
Packaging Options(3)
90 TABLET, COATED in 1 BOTTLE (72241-077-04)
1000 TABLET, COATED in 1 BOTTLE (72241-077-11)
30 TABLET, COATED in 1 BOTTLE (72241-077-22)