NDC 70954-275 – Fluphenazine Hydrochloride

Fluphenazine Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70954-275

Product details

Brand name
Fluphenazine Hydrochloride
Generic name
Fluphenazine Hydrochloride
Labeler
ANI Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA214674
Marketed since
March 1, 2021
Listing expires
December 31, 2026
Pharmacologic class
Phenothiazine

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
70954-275-10100 TABLET in 1 BOTTLE (70954-275-10)Mar 1, 2021
70954-275-20500 TABLET in 1 BOTTLE (70954-275-20)Mar 1, 2021

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