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
- 71205-837_bc22941e-d2e7-4165-91ea-7239c8b9882d
- Product NDC
- 71205-837
- Form
- TABLET, FILM COATED
- Composition / generic term
- Fluphenazine Hydrochloride
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220801
- Source listing expiry
- 20261231
Source-listed ingredients
- FLUPHENAZINE HYDROCHLORIDE — 1 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-00) · 71205-837-00
- 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-11) · 71205-837-11
- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-30) · 71205-837-30
- 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-55) · 71205-837-55
- 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-60) · 71205-837-60
- 240 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-64) · 71205-837-64
- 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-72) · 71205-837-72
- 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-78) · 71205-837-78
- 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-90) · 71205-837-90
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 →