NDC 50111-647 – Fluoxetine

Fluoxetine Hydrochloride 10 mg/1 · Capsule · Oral

Human Prescription Drug 4 recalls

Product NDC50111-647

Product details

Brand name
Fluoxetine
Generic name
Fluoxetine
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA076001
Marketed since
January 29, 2002
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Fluoxetine →

Package NDC codes (3)

Package NDCDescriptionSince
50111-647-01100 CAPSULE in 1 BOTTLE (50111-647-01)Jan 29, 2002
50111-647-02500 CAPSULE in 1 BOTTLE (50111-647-02)Jan 29, 2002
50111-647-031000 CAPSULE in 1 BOTTLE (50111-647-03)Jan 29, 2002

Recalls mentioning this NDC

Other Fluoxetine products