Venlafaxine Hydrochloride 71335-2992
Product NDC
71335-2992- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 25, 2023
- Listing Expires
- December 31, 2027
- Application
- ANDA217390
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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(4)
30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-2992-1)
60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-2992-2)
90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-2992-3)
100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-2992-4)