United States · FDA National Drug Code directory
Cyproheptadine 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
- 71335-2368_e672afab-de82-4aa0-9d12-f1d7d21dc6c7
- Product NDC
- 71335-2368
- Form
- TABLET
- Composition / generic term
- Cyproheptadine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150729
- Source listing expiry
- 20261231
Source-listed ingredients
- CYPROHEPTADINE HYDROCHLORIDE — 4 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (71335-2368-1) · 71335-2368-1
- 60 TABLET in 1 BOTTLE (71335-2368-2) · 71335-2368-2
- 28 TABLET in 1 BOTTLE (71335-2368-3) · 71335-2368-3
- 100 TABLET in 1 BOTTLE (71335-2368-4) · 71335-2368-4
- 90 TABLET in 1 BOTTLE (71335-2368-5) · 71335-2368-5
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 →