Desvenlafaxine Er 61919-0882
Product NDC
61919-0882- Manufacturer
- Direct_rx
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 4, 2019
- Listing Expires
- December 31, 2027
- Application
- ANDA204172
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Desvenlafaxine Succinate | 50 mg/1 |
Drug Class
Cytochrome P450 2D6 Inhibitors [MoA]Norepinephrine Uptake Inhibitors [MoA]Serotonin Uptake Inhibitors [MoA]
Packaging Options(3)
28 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (61919-882-28)
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (61919-882-30)
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (61919-882-60)