NDC 0121-0885

Prednisolone 15 mg per 5 mL solution

On the label: Pharmaceutical Associates, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI PharmaGreenville, SC, United StatesMakes it, tests it, packages it and labels it No problems foundAug 1, 2025 · 18 inspections, 1 with FDA action

Product details

Generic drug
Prednisolone: every company that makes it
Form
solution, oral
Strength
15 mg per 5 mL
Approval
ANDA ANDA040571
On the market since
Sep 12, 2023
Package NDCs
0121-0885-08 0121-0885-16
Official label
DailyMed (National Library of Medicine), updated Aug 19, 2024

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