NDC 50090-2098
Depo-Medrol 40 mg per 1 mL injection, suspension
On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions rebottles it from Pharmacia & Upjohn Company LLC's NDC 0009-3073.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Pharmacia & Upjohn Company LLC | Kalamazoo, MI, United States | Makes it, makes the active ingredient, tests it, packages it and labels it | Problems found, fixed voluntarilyJun 16, 2023 · 9 inspections |
| Sterigenics Belgium (Petit Rechain) SRL | Verviers, Belgium | Sterilizes it | Problems found, fixed voluntarilyJun 29, 2023 · 3 inspections |
Repackaging site
- A-S Medication Solutions LLC, Libertyville, IL, United States · relabels it
Recalls
- Apr 13, 2022 · Class II · Mckesson Medical-Surgical Inc. Corporate Office
cGMP deviations: Temperature abuse
Lots: McKesson Medical-Surgical (MMS) is not able to identify the particular lot number received by a particular consignee for the recalled prescription products. Each letter includes the date it was distributed to customers and the dates that impacted product may have been shipped to the customer. - Apr 13, 2022 · Class II · Mckesson Medical-Surgical Inc. Corporate Office
cGMP deviations: Temperature abuse
Lots: McKesson Medical-Surgical (MMS) is not able to identify the particular lot number received by a particular consignee for the recalled prescription products. Each letter includes the date it was distributed to customers and the dates that impacted product may have been shipped to the customer. - Jul 30, 2014 · Class III · Pfizer Inc.
Failed pH Specification: A pH result of 2.9 was obtained at the 9 month stability test interval at 25C/60%RH. The registered specification for pH is 3.0 - 7.0
Lots: Lot H43272, H43265 Exp. 09/14
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
- injection, suspension, intra-articular; intralesional; intramuscular; soft tissue
- Strength
- 40 mg per 1 mL
- Approval
- NDA NDA011757
- On the market since
- May 28, 1959
- Package NDCs
50090-2098-0- Official label
- DailyMed (National Library of Medicine), updated Nov 6, 2025
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