Venlafaxine Hydrochloride 47335-0760
Product NDC
47335-0760- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 15, 2014
- Listing Expires
- December 31, 2026
- Application
- ANDA091272
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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(6)
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-760-08)
1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-760-18)
10 BLISTER PACK in 1 BOX, UNIT-DOSE (47335-760-61) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-760-81)
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-760-83)
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-760-88)