Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Akorn | Location not on file | Makes it and labels it | Not inspected on record |
Recalls
- Dec 15, 2017 · Class III · Akorn Inc
CGMP Deviations: Inadvertent release of a drug product with unapproved active ingredient manufacturer.
Lots: Batch# 359774; Exp. 09/02/19
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Gabapentin: every company that makes it
- Form
- solution
- Strength
- 250 mg per 5 mL
- Approval
- ANDA ANDA078974
- On the market since
- Feb 23, 2011
- Package NDCs
50383-311-47- Official label
- DailyMed (National Library of Medicine), updated Mar 14, 2022
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?