Fluoxetine Hydrochloride 00832-6032-12

Package NDC

00832-6032-12

Manufacturer: Upsher-Smith Laboratories, Llc
Dosage Form: For Solution
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: November 15, 2022
Listing Expires: December 31, 2026
Application: ANDA216953

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Active Ingredients

Ingredient	Strength
Fluoxetine Hydrochloride	20 mg/5mL

Drug Class

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

Selected Package

00832-6032-12Selected

1 BOTTLE in 1 CARTON (0832-6032-12) / 120 mL in 1 BOTTLE