Fluphenazine Hydrochloride 51672-4233-01

Package NDC

51672-4233-01

Manufacturer: Sun Pharmaceutical Industries, Inc.
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: April 14, 2022
Listing Expires: December 31, 2027
Application: ANDA215674

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Active Ingredients

Ingredient	Strength
Fluphenazine Hydrochloride	1 mg/1

Drug Class

Phenothiazine [EPC]Phenothiazines [CS]

Selected Package

51672-4233-01Selected

1 BOTTLE in 1 CARTON (51672-4233-1) / 100 TABLET, FILM COATED in 1 BOTTLE