NDC 62135-236

Cyproheptadine Hydrochloride 4 mg tablet

On the label: Chartwell RX, LLC..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Chartwell Pharmaceuticals Congers, LLC.Congers, NY, United StatesMakes it, tests it, packages it and labels it Serious problems, FDA actionNov 18, 2025 · 8 inspections, 2 with FDA action

Product details

Generic drug
Cyproheptadine: every company that makes it
Form
tablet, oral
Strength
4 mg
Approval
ANDA ANDA088212
On the market since
May 26, 1983
Package NDCs
62135-236-90
Official label
DailyMed (National Library of Medicine), updated Jan 27, 2023

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