NDC 68788-7909 – Fluoxetine

Fluoxetine Hydrochloride 20 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC68788-7909

Product details

Brand name
Fluoxetine
Generic name
Fluoxetine Hydrochloride
Labeler
Preferred Pharmaceuticals, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA204597
Marketed since
May 18, 2021
Listing expires
December 31, 2027
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Fluoxetine →

Package NDC codes (4)

Package NDCDescriptionSince
68788-7909-1100 CAPSULE in 1 BOTTLE (68788-7909-1)May 18, 2021
68788-7909-330 CAPSULE in 1 BOTTLE (68788-7909-3)May 18, 2021
68788-7909-660 CAPSULE in 1 BOTTLE (68788-7909-6)May 18, 2021
68788-7909-990 CAPSULE in 1 BOTTLE (68788-7909-9)May 18, 2021

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