NDC 46708-243 – Fluoxetine Hydrochloride

Fluoxetine Hydrochloride 20 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC46708-243

Product details

Brand name
Fluoxetine Hydrochloride
Generic name
Fluoxetine Hydrochloride
Labeler
Alembic Pharmaceuticals Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA208698
Marketed since
April 15, 2017
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Fluoxetine hydrochloride →

Package NDC codes (3)

Package NDCDescriptionSince
46708-243-3030 TABLET, FILM COATED in 1 BOTTLE (46708-243-30)Apr 15, 2017
46708-243-31100 TABLET, FILM COATED in 1 BOTTLE (46708-243-31)Apr 15, 2017
46708-243-911000 TABLET, FILM COATED in 1 BOTTLE (46708-243-91)Apr 15, 2017

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