NDC 67296-1656
Prednisolone 15 mg per 5 mL solution
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Akorn's NDC 50383-042.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Akorn | Location not on file | Makes it | Not inspected on record |
Repackaging site
- EPM Packaging, Location not on file · repackages it
Recalls
- Aug 1, 2022 · Class II · Akorn, Inc
Defective Container: Product has incomplete induction seals.
Lots: Lot# 379804, Exp. 8/31/2023
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Prednisolone: every company that makes it
- Form
- solution
- Strength
- 15 mg per 5 mL
- Approval
- ANDA ANDA040401
- On the market since
- Feb 27, 2003
- Package NDCs
67296-1656-6- Official label
- DailyMed (National Library of Medicine), updated Aug 9, 2024
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