Fluoxetine Hydrochloride 49884-0335-11

Package NDC

49884-0335-11

Manufacturer: Endo Usa, Inc.
Dosage Form: Tablet, Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: August 22, 2016
Listing Expires: December 31, 2026
Application: ANDA203836

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Active Ingredients

Ingredient	Strength
Fluoxetine Hydrochloride	10 mg/1

Drug Class

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

Selected Package

49884-0335-11Selected

30 TABLET, COATED in 1 BOTTLE, PLASTIC (49884-335-11)

Other packages for this product(1)

49884-0335-01

100 TABLET, COATED in 1 BOTTLE, PLASTIC (49884-335-01)

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