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
- 72789-102_4af611bc-838d-98d2-e063-6294a90a74d8
- Product NDC
- 72789-102
- Form
- TABLET
- Composition / generic term
- Cyproheptadine Hydrochloride
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200301
- 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 (72789-102-01) · 72789-102-01
- 30 TABLET in 1 BOTTLE, PLASTIC (72789-102-30) · 72789-102-30
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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