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Class II · ModerateActive recall

Cyproheptadine Hydrochloride

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLots: Batch # CR2518, Exp. 11/2027; Batch # CR2601, Exp. 12/2027; CR2602, CR2603, Exp. 01/2028; CR2604, CR2605, Exp. 02/2028.
Where it was soldNationwide U.S.A.
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

Presence of Precipitate: medication was crystallizing and particles floating in the bottle

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byLyne Laboratories, Inc., Brockton, MA
Brand nameCYPROHEPTADINE HYDROCHLORIDE
Generic nameCYPROHEPTADINE HYDROCHLORIDE
Active ingredient(s)CYPROHEPTADINE HYDROCHLORIDE
Distributed by / forRising Pharma Holdings, Inc., East Brunswick, NJ
NDC64980-504-48
Show the full FDA record
Full product labelRising, Cyproheptadine Hydrochloride Syrup, 2mg/5 mL, 473 mL (ONE PINT), Rx only, Manufactured for: Rising Pharma Holdings, Inc., East Brunswick, NJ, Manufactured by: Lyne Laboratories, Inc., Brockton, MA. NDC 64980-504-48.
Recalling firmRising Pharma Holding, Inc.
DistributionNationwide U.S.A.
Quantity74208 units
Recall initiated2026-07-13
Report date2026-07-29
Recall completed—
Recall numberD-0724-2026
ClassificationClass II
FDA statusOngoing
Origin on fileEast Brunswick NJ United States

Related

Recent drug recallsCheck another medication

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.