NDC 70518-2518
Acyclovir 800 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Camber Pharmaceuticals Inc.'s NDC 31722-778.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hetero Labs Limited | Mahabubnagar, India | Makes it | Problems found, fixed voluntarilyAug 12, 2022 · 5 inspections, 1 with FDA action |
Recalls
- Apr 27, 2017 · Class III · Hetero USA Inc
Presence of Foreign Substance: human hair melded into tablet.
Lots: Lot # ACY16075 Exp. 09/2018
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
- tablet, oral
- Strength
- 800 mg
- Approval
- ANDA ANDA203834
- On the market since
- Jan 1, 2020
- Package NDCs
70518-2518-070518-2518-170518-2518-270518-2518-370518-2518-4- Official label
- DailyMed (National Library of Medicine), updated Jul 24, 2026
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