Venlafaxine 57664-0392-88

Package NDC

57664-0392-88

Manufacturer: Sun Pharmaceutical Industries, Inc.
Dosage Form: Tablet
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: June 13, 2008
Listing Expires: December 31, 2027
Application: ANDA078627

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Active Ingredients

Ingredient	Strength
Venlafaxine Hydrochloride	25 mg/1

Drug Class

Norepinephrine Uptake Inhibitors [MoA]Serotonin Uptake Inhibitors [MoA]Serotonin and Norepinephrine Reuptake Inhibitor [EPC]

Selected Package

57664-0392-88Selected

100 TABLET in 1 BOTTLE (57664-392-88)