NDC 61919-291
Prednisolone 15 mg per 5 mL solution
On the label: Direct Rx. It's repackaged: Direct Rx 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
- Direct Rx, Dawsonville, GA, United States · relabels 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
- Jan 1, 2014
- Package NDCs
61919-291-37- Official label
- DailyMed (National Library of Medicine), updated Jan 21, 2020
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?