NDC 0121-0654 – Fluphenazine Hydrochloride

Fluphenazine Hydrochloride .5 mg/mL · Elixir · Oral

Human Prescription Drug

Product NDC0121-0654

Product details

Brand name
Fluphenazine Hydrochloride
Generic name
Fluphenazine Hydrochloride
Labeler
PAI Holdings, LLC dba PAI Pharma
Dosage form
Elixir
Route
Oral
Marketing category
ANDA · ANDA040146
Marketed since
August 31, 2010
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
0121-0654-0260 mL in 1 BOTTLE (0121-0654-02)Aug 31, 2010
0121-0654-16473 mL in 1 BOTTLE (0121-0654-16)Aug 31, 2010

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