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
- 52817-210_02c5c6cb-c0be-4b61-855e-1b8f4e4785b0
- Product NDC
- 52817-210
- Form
- TABLET
- Composition / generic term
- Cyproheptadine Hydrochloride
- Labeler
- TRUPHARMA, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170117
- Source listing expiry
- 20271231
Source-listed ingredients
- CYPROHEPTADINE HYDROCHLORIDE — 4 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE, PLASTIC (52817-210-10) · 52817-210-10
- 500 TABLET in 1 BOTTLE, PLASTIC (52817-210-50) · 52817-210-50
Source and coverage
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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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