NDC 71335-0695
Acyclovir 800 mg tablet
On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack 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 |
Repackaging site
- Bryant Ranch Prepack, Burbank, CA, United States · repackages it and relabels it
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
- Nov 29, 2013
- Package NDCs
71335-0695-071335-0695-171335-0695-271335-0695-371335-0695-471335-0695-571335-0695-671335-0695-771335-0695-871335-0695-9- Official label
- DailyMed (National Library of Medicine), updated Jun 4, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?