NDC 55111-150 – Fluoxetine

Fluoxetine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC55111-150

Product details

Brand name
Fluoxetine
Generic name
Fluoxetine
Labeler
Dr.Reddy's Laboratories Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076006
Marketed since
September 30, 2016
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Fluoxetine →

Package NDC codes (5)

Package NDCDescriptionSince
55111-150-01100 TABLET, FILM COATED in 1 BOTTLE (55111-150-01)Sep 30, 2016
55111-150-05500 TABLET, FILM COATED in 1 BOTTLE (55111-150-05)Sep 30, 2016
55111-150-101000 TABLET, FILM COATED in 1 BOTTLE (55111-150-10)Sep 30, 2016
55111-150-3030 TABLET, FILM COATED in 1 BOTTLE (55111-150-30)Sep 30, 2016
55111-150-7810 BLISTER PACK in 1 CARTON (55111-150-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-150-79)Sep 30, 2016

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