Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Akorn | Location not on file | Makes it | Not inspected on record |
Recalls
- Oct 28, 2013 · Class III · Hi-Tech Pharmacal Co., Inc.
Failed Stability Specification; product viscosity and or pH are below specification.
Lots: Batch no: 1) 614463 (exp. 03/2014), 2) 612905 (exp. 12/2013), 3) 614923 (exp. 03/2014), 4) 615852 (exp. 05/2014), 5) 615855 (exp. 05/2014), 6) 616689 (exp. 07/2014), 7) 616692 (exp. 07/2014).
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Acyclovir: every company that makes it
- Form
- suspension
- Strength
- 200 mg per 5 mL
- Approval
- ANDA ANDA077026
- On the market since
- Jun 7, 2005
- Package NDCs
50383-810-16- Official label
- DailyMed (National Library of Medicine), updated Sep 19, 2022
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