NDC 16571-805

Cyproheptadine Hydrochloride 4 mg tablet

On the label: Rising Pharma Holdings, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
InvaTech Pharma Solutions LLCEast Brunswick, NJ, United StatesMakes it, tests it and packages it Problems found, fixed voluntarilyMay 13, 2026 · 4 inspections

Product details

Generic drug
Cyproheptadine: every company that makes it
Form
tablet, oral
Strength
4 mg
Approval
ANDA ANDA207555
On the market since
Feb 9, 2022
Package NDCs
16571-805-01 16571-805-10
Official label
DailyMed (National Library of Medicine), updated Feb 8, 2022

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