NDC 84549-155
Acyclovir Sodium 1000 mg per 20 mL injection, solution
On the label: ProPharma Distribution. It's repackaged: ProPharma Distribution rebottles it from AuroMedics Pharma LLC's NDC 55150-155.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Eugia Pharma Specialities Limited | Sangareddy, India | Makes it, tests it and packages it | Serious problems, FDA actionFeb 6, 2026 · 7 inspections, 2 with FDA action |
Repackaging site
- ProPharma Distribution, Westminster, CO, United States · repackages it and relabels it
Recalls
- Dec 28, 2022 · Class II · Eugia US LLC
Presence of Particulate Matter: Customer complaint of dark particles found inside the vial
Lots: Lot # AC22004, Expiry: 08/2023 - Sep 26, 2022 · Class II · AuroMedics Pharma LLC
Presence of Particulate Matter: Customer complaint for a dark red, brown and black particulate floating inside vial.
Lots: Lot: AC22006, Exp 08/2023
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Acyclovir: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 1000 mg per 20 mL
- Approval
- ANDA ANDA203701
- On the market since
- Oct 11, 2013
- Package NDCs
84549-155-20- Official label
- DailyMed (National Library of Medicine), updated Jul 18, 2025
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