Fluoxetine Hydrochloride 16714-0114-01

Package NDC

16714-0114-01

Manufacturer: Northstar Rx Llc
Dosage Form: Tablet, Film Coated
Route: Oral And Oral
Product Type: Human Prescription Drug
Marketing Start: September 18, 2019
Listing Expires: December 31, 2026
Application: ANDA211721

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Active Ingredients

Ingredient	Strength
Fluoxetine Hydrochloride	60 mg/1

Drug Class

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

Selected Package

16714-0114-01Selected

30 TABLET, FILM COATED in 1 BOTTLE (16714-114-01)