Venlafaxine 68084-0856
Product NDC
68084-0856- Manufacturer
- American Health Packaging
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 6, 2015
- Listing Expires
- December 31, 2026
- Application
- ANDA077653
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Venlafaxine Hydrochloride | 75 mg/1 |
Drug Class
Norepinephrine Uptake Inhibitors [MoA]Serotonin Uptake Inhibitors [MoA]Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
Packaging Options(1)
100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-856-01) / 1 TABLET in 1 BLISTER PACK (68084-856-11)