NDC 68084-215
Valacyclovir Hydrochloride 500 mg tablet, film coated
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from Aurobindo Pharma Limited's NDC 65862-448.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Apl Healthcare Limited | Tirupati, India | Makes it and tests it | Problems found, fixed voluntarilyDec 17, 2025 · 5 inspections |
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action |
| Aurolife Pharma LLC | Dayton, NJ, United States | Makes it | Serious problems, FDA actionDec 7, 2021 · 10 inspections, 1 with FDA action |
| Aurolife Pharma LLC | Dayton, NJ, United States | Packages it and labels it | Serious problems, FDA actionDec 7, 2021 · 10 inspections, 1 with FDA action |
Repackaging site
- American Health Packaging, Columbus, OH, United States · repackages it
Product details
- Generic drug
- Acyclovir: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 500 mg
- Approval
- ANDA ANDA090682
- On the market since
- Aug 20, 2014
- Package NDCs
68084-215-0168084-215-1168084-215-21- Official label
- DailyMed (National Library of Medicine), updated Oct 23, 2026
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