NDC 68151-1728
Cyproheptadine Hydrochloride 2 mg per 5 mL syrup
On the label: Carilion Materials Management. It's repackaged: Carilion Materials Management rebottles it from Rising Pharma Holdings, Inc.'s NDC 64980-504.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lyne Laboratories, Inc. | Brockton, MA, United States | Makes it | Problems found, fixed voluntarilyMar 10, 2026 · 9 inspections, 1 with FDA action |
Repackaging site
- Carilion Materials Management, Roanoke, Virginia, United States · repackages it
Recalls
- Jul 13, 2026 · Class II · Rising Pharma Holding, Inc.
Presence of Precipitate: medication was crystallizing and particles floating in the bottle
Lots: Lots: Batch # CR2518, Exp. 11/2027; Batch # CR2601, Exp. 12/2027; CR2602, CR2603, Exp. 01/2028; CR2604, CR2605, Exp. 02/2028.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Cyproheptadine: every company that makes it
- Form
- syrup
- Strength
- 2 mg per 5 mL
- Approval
- ANDA ANDA040668
- On the market since
- Jul 10, 2006
- Package NDCs
68151-1728-7- Official label
- DailyMed (National Library of Medicine), updated Aug 11, 2011
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