NDC 51672-4236 – Fluphenazine Hydrochloride

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

Human Prescription Drug

Product NDC51672-4236

Product details

Brand name
Fluphenazine Hydrochloride
Generic name
Fluphenazine Hydrochloride
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215674
Marketed since
April 14, 2022
Listing expires
December 31, 2027
Pharmacologic class
Phenothiazine

Active ingredients

Uses, dosage, side effects and warnings for Fluphenazine Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
51672-4236-1100 TABLET, FILM COATED in 1 BOTTLE (51672-4236-1)Apr 14, 2022

Other Fluphenazine Hydrochloride products