NDC 69306-004
Methylprednisolone 4 mg tablet
On the label: Doc Rx. It's repackaged from NDC 59746-001, made by Jubilant Cadista Pharmaceuticals Inc. (Methylprednisolone). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Jubilant Cadista Pharmaceuticals, Inc. | Location not on file | Makes it | Not inspected on record |
| Asclemed USA Inc. dba Enovachem | Torrance, CA, United States | Repackages it | No problems foundMar 5, 2025 · 6 inspections, 1 with FDA action |
Recalls
- Mar 19, 2021 · Class III · Asclemed USA Inc. dba Enovachem Pharmaceuticals
Labeling: Illegible label: Manufacturer received complaint of mis-alignment print of the printed dosing instructions on the blister card.
Lots: Lot #: 20K0043P, Exp. 8/31/2022; 20L0026P, Exp. 9/30/2022
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
- Strength
- 4 mg
- Approval
- ANDA ANDA040189
- On the market since
- Oct 31, 1997
- Package NDCs
69306-004-21- Official label
- DailyMed (National Library of Medicine), updated Oct 21, 2022
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?