Fluphenazine Hydrochloride 70954-0273-10

Package NDC

70954-0273-10

Manufacturer: Ani Pharmaceuticals, Inc.
Dosage Form: Tablet
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: March 1, 2021
Listing Expires: December 31, 2026
Application: ANDA214674

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Active Ingredients

Ingredient	Strength
Fluphenazine Hydrochloride	1 mg/1

Drug Class

Phenothiazine [EPC]Phenothiazines [CS]

Selected Package

70954-0273-10Selected

100 TABLET in 1 BOTTLE (70954-273-10)