NDC 13668-473 – Fluoxetine

Fluoxetine Hydrochloride 20 mg/1 · Tablet · Oral

Human Prescription Drug 2 recalls

Product NDC13668-473

Product details

Brand name
Fluoxetine
Generic name
Fluoxetine
Labeler
Torrent Pharmaceuticals Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA206937
Marketed since
October 21, 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
13668-473-01100 TABLET in 1 BOTTLE (13668-473-01)Oct 21, 2016
13668-473-101000 TABLET in 1 BOTTLE (13668-473-10)Oct 21, 2016
13668-473-3030 TABLET in 1 BOTTLE (13668-473-30)Oct 21, 2016
13668-473-74100 TABLET in 1 CARTON (13668-473-74)Oct 21, 2016
13668-473-9128 TABLET in 1 CARTON (13668-473-91)Oct 21, 2016

Recalls mentioning this NDC

Other Fluoxetine products