NDC 52817-415

Cyproheptadine Hydrochloride 4 mg tablet

On the label: TruPharma LLC..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Appco Pharma LLCPiscataway, NJ, United StatesMakes it, tests it and packages it Problems found, fixed voluntarilyMay 14, 2026 · 9 inspections

Product details

Generic drug
Cyproheptadine: every company that makes it
Form
tablet, oral
Strength
4 mg
Approval
ANDA ANDA206553
On the market since
Jun 1, 2026
Package NDCs
52817-415-10 52817-415-50
Official label
DailyMed (National Library of Medicine), updated Jul 14, 2026

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