Fluoxetine Hydrochloride 55111-0284

Product NDC

55111-0284

Manufacturer: Dr.reddy's Laboratories Limited
Dosage Form: Capsule, Delayed Release Pellets
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: March 24, 2010
Listing Expires: December 31, 2026
Application: ANDA078572

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Active Ingredients

Ingredient	Strength
Fluoxetine Hydrochloride	90 mg/1

Drug Class

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

Packaging Options(1)

55111-0284-48

1 BLISTER PACK in 1 CARTON (55111-284-48) / 4 CAPSULE, DELAYED RELEASE PELLETS in 1 BLISTER PACK

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