NDC 68084-149
Methylprednisolone 4 mg tablet
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from Par Health USA, LLC's NDC 0603-4593.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Generics Bidco II LLC d/b/a Prinston Laboratories | Charlotte, NC, United States | Makes it, packages it and labels it | Problems found, fixed voluntarilySep 19, 2025 · 10 inspections, 1 with FDA action |
| Par Formulations Private Limited | Chennai, India | Makes it, tests it and packages it | Problems found, fixed voluntarilyJun 10, 2026 · 7 inspections |
Repackaging site
- American Health Packaging, Columbus, OH, United States · repackages it
Recalls
- Oct 10, 2014 · Class III · American Health Packaging
Subpotent; 6 month stability time point
Lots: AHP Lot #: 134124 and 140364 Expiration Date of both lots: 05/2015 Carton NDC #: 68084-149-01 Single Dose NDC #: 68084-149-11 - Sep 11, 2014 · Class III · Qualitest Pharmaceuticals
Subpotent; 6 month stability time point
Lots: 100 count: T147F13A, Exp. 05/2015; 21 count: S003M14, Exp. 05/2015
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 ANDA040183
- On the market since
- Dec 3, 2013
- Package NDCs
68084-149-0168084-149-11- Official label
- DailyMed (National Library of Medicine), updated Jul 1, 2026
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