Eugia Pharma Specialities Limited
Sangareddy, India · makes it, tests it and packages it
Serious problems, FDA action Last FDA inspection Feb 6, 2026. 7 inspections on record, 2 with serious problems.
NDC 55150-155
Acyclovir Sodium 1000 mg per 20 mL injection, solution
On the label: AuroMedics Pharma LLC.
Where it's made
Recalls
- Dec 28, 2022 · Class II · Ongoing
Presence of Particulate Matter: Customer complaint of dark particles found inside the vial
Lots: Lot # AC22004, Expiry: 08/2023 - Sep 26, 2022 · Class II · Completed
Presence of Particulate Matter: Customer complaint for a dark red, brown and black particulate floating inside vial.
Lots: Lot: AC22006, Exp 08/2023
Product details
- Generic drug
- Acyclovir: see 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
55150-155-20- Official label
- DailyMed (National Library of Medicine), updated Jul 5, 2023
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