NDC 50268-062
Acyclovir 800 mg tablet
On the label: AvPAK. It's repackaged: AvPAK 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 |
Recalls
- Feb 9, 2018 · Class II · Apace KY LLC
Presence of Foreign Tablet/Capsule; cartons labeled to contain Acyclovir tablets may contain Torsemide tablets in some of the blister cavities.
Lots: Lot: 19900, exp 05/2019
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 ANDA075382
- On the market since
- Jul 18, 2014
- Package NDCs
50268-062-1150268-062-15- Official label
- DailyMed (National Library of Medicine), updated Jan 8, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?