NDC 71205-388
Acyclovir 800 mg tablet
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.'s NDC 23155-228.
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
- Proficient Rx LP, Thousand Oaks, CA, United States · repackages it and relabels 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
- 800 mg
- Approval
- ANDA ANDA074891
- On the market since
- Aug 8, 2013
- Package NDCs
71205-388-3071205-388-3571205-388-6071205-388-90- Official label
- DailyMed (National Library of Medicine), updated Feb 1, 2022
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