United States · FDA National Drug Code directory
Fluphenazine Hydrochoride
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
- 70518-4691_55b89c3d-bcb4-01ee-e063-6394a90a7f03
- Product NDC
- 70518-4691
- Form
- TABLET, FILM COATED
- Composition / generic term
- fluphenazine hydrochloride
- Labeler
- REMEDYREPACK INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260703
- Source listing expiry
- 20271231
Source-listed ingredients
- FLUPHENAZINE HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 POUCH in 1 BOX (70518-4691-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4691-1) · 70518-4691-0
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 →