NDC 53002-0271
Acyclovir 800 mg tablet
On the label: RPK Pharmaceuticals, Inc.. It's repackaged: RPK Pharmaceuticals, Inc. rebottles it from Carlsbad Technology, Inc.'s NDC 61442-113.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Carlsbad Technology, Inc. | Carlsbad, CA, United States | Makes it and tests it | Problems found, fixed voluntarilyJun 30, 2026 · 12 inspections |
Repackaging site
- RPK Pharmaceuticals, Inc., Union City, California, United States · repackages it and relabels it
Product details
- Generic drug
- Acyclovir: every company that makes it
- Form
- tablet
- Strength
- 800 mg
- Approval
- ANDA ANDA075382
- On the market since
- Oct 22, 2009
- Package NDCs
53002-0271-053002-0271-153002-0271-253002-0271-353002-0271-453002-0271-553002-0271-6- Official label
- DailyMed (National Library of Medicine), updated Jun 7, 2023
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