NDC 27241-255 – Fluphenazine hydrochloride

Fluphenazine Hydrochloride 1 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC27241-255

Product details

Brand name
Fluphenazine hydrochloride
Generic name
Fluphenazine hydrochloride
Labeler
Ajanta Pharma USA Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA217410
Marketed since
January 5, 2023
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
27241-255-01100 TABLET in 1 BOTTLE (27241-255-01)Jan 5, 2023

Recalls mentioning this NDC

Other Fluphenazine Hydrochloride products