NDC 70752-232

Cyproheptadine Hydrochloride 2 mg tablet

On the label: Quagen Pharmaceuticals LLC.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Quagen Pharmaceuticals LLCWest Caldwell, NJ, United StatesMakes it and packages it No problems foundApr 17, 2026 · 3 inspections

Product details

Generic drug
Cyproheptadine: every company that makes it
Form
tablet, oral
Strength
2 mg
Approval
ANDA ANDA212491
On the market since
Oct 15, 2026
Package NDCs
70752-232-03 70752-232-05
Official label
DailyMed (National Library of Medicine), updated Oct 6, 2026

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