Fluphenazine Hydrochloride 00904-7160-61

Package NDC

00904-7160-61

Manufacturer: Major Pharmaceuticals
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: August 25, 1988
Listing Expires: December 31, 2026
Application: ANDA089743

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Active Ingredients

Ingredient	Strength
Fluphenazine Hydrochloride	10 mg/1

Drug Class

Phenothiazine [EPC]Phenothiazines [CS]

Selected Package

00904-7160-61Selected

100 BLISTER PACK in 1 CARTON (0904-7160-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK