Venlafaxine Hydrochloride 33342-0194
Product NDC
33342-0194- Manufacturer
- Macleods Pharmaceuticals Limited
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 6, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA204889
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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(5)
30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (33342-194-07)
90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (33342-194-10)
100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (33342-194-11)
10 BLISTER PACK in 1 CARTON (33342-194-12) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK
500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (33342-194-15)