United States · FDA National Drug Code directory

Fluphenazine Hydrochloride

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
0121-0654_be2cdaa4-74b5-4256-90c0-e1410973b3f5
Product NDC
0121-0654
Form
ELIXIR
Composition / generic term
Fluphenazine Hydrochloride
Labeler
PAI Holdings, LLC dba PAI Pharma
Marketing category
ANDA
Marketing start / end (source format)
20100831
Source listing expiry
20261231

Source-listed ingredients

  • FLUPHENAZINE HYDROCHLORIDE — .5 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 60 mL in 1 BOTTLE (0121-0654-02) · 0121-0654-02
  • 473 mL in 1 BOTTLE (0121-0654-16) · 0121-0654-16

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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Fluphenazine Hydrochloride — United States | Molindra Medicines