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
- 69238-1681_e350dbeb-6212-43b1-8c85-f60fb1719e0f
- Product NDC
- 69238-1681
- Form
- TABLET, FILM COATED
- Composition / generic term
- fluphenazine hydrochloride
- Labeler
- Amneal Pharmaceuticals NY LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200711
- Source listing expiry
- 20271231
Source-listed ingredients
- FLUPHENAZINE HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69238-1681-1) · 69238-1681-1
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.
Browse United States records →