Fluoxetine 49483-0701

Generic: Fluoxetine Hydrochloride

Product NDC

49483-0701

Manufacturer: Time Cap Laboratories, Inc.
Dosage Form: Capsule
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: February 12, 2022
Listing Expires: December 31, 2026
Application: ANDA075465

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Active Ingredients

Ingredient	Strength
Fluoxetine Hydrochloride	10 mg/1

Drug Class

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

Packaging Options(2)

49483-0701-01

100 CAPSULE in 1 BOTTLE (49483-701-01)

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49483-0701-10

1000 CAPSULE in 1 BOTTLE (49483-701-10)

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