NDC 80425-0231

Methylprednisolone 4 mg tablet

On the label: Advanced Rx Pharmacy of Tennessee, LLC. It's repackaged: Advanced Rx Pharmacy of Tennessee, LLC rebottles it from Zydus Pharmaceuticals (USA) Inc.'s NDC 68382-916.

India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Zydus Lifesciences LimitedAhmedabad, IndiaMakes it and tests it Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action

Repackaging site

Recalls

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug
Methylprednisolone: every company that makes it
Form
tablet, oral
Strength
4 mg
Approval
ANDA ANDA206751
On the market since
Jan 11, 2023
Package NDCs
80425-0231-1
Official label
DailyMed (National Library of Medicine), updated Dec 31, 2024

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