NDC 0121-1038

Megestrol Acetate 400 mg per 10 mL suspension

On the label: Pharmaceutical Associates, Inc.. It's repackaged: Pharmaceutical Associates, Inc. rebottles it from ANI Pharmaceuticals, Inc.'s NDC 70954-896.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Novitium Pharma LLCEast Windsor, NJ, United StatesMakes it, tests it, packages it and labels it No problems foundFeb 16, 2024 · 5 inspections

Product details

Generic drug
Megestrol: every company that makes it
Form
suspension, oral
Strength
400 mg per 10 mL
Approval
ANDA ANDA077404
On the market since
Oct 17, 2025
Package NDCs
0121-1038-00 0121-1038-10 0121-1038-40
Official label
DailyMed (National Library of Medicine), updated Oct 17, 2025

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