NDC 68071-2279
Acyclovir 400 mg tablet
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.'s NDC 23155-227.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Labs Inc. | East Brunswick, NJ, United States | Makes it, tests it, packages it and labels it | No problems foundSep 19, 2023 · 10 inspections |
| Recordati Industria Chimica E Farmaceutica SpA | Campoverde di Aprilia (Latina), Italy | Makes the active ingredient | Problems found, fixed voluntarilyOct 3, 2025 · 6 inspections |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · repackages it
Recalls
- Apr 21, 2021 · Class III · Heritage Pharmaceuticals Inc
Labeling: Incorrect or Missing Lot and/or Exp Date
Lots: Lot A120036, Exp DEC 2023
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
- 400 mg
- Approval
- ANDA ANDA074891
- On the market since
- Aug 8, 2013
- Package NDCs
68071-2279-8- Official label
- DailyMed (National Library of Medicine), updated Jul 17, 2024
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