NDC 50090-6129

Cyproheptadine Hydrochloride 4 mg tablet

On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions rebottles it from Zydus Pharmaceuticals (USA) Inc.'s NDC 70710-1110.

India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Zydus Lifesciences LimitedAhmedabad, IndiaMakes it and tests it Problems found, fixed voluntarilyMar 24, 2023 · 5 inspections

Repackaging site

Product details

Generic drug
Cyproheptadine: every company that makes it
Form
tablet, oral
Strength
4 mg
Approval
ANDA ANDA208938
On the market since
Jul 20, 2017
Package NDCs
50090-6129-1
Official label
DailyMed (National Library of Medicine), updated Nov 2, 2023

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?