NDC 63187-366
acyclovir 800 mg tablet
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Zydus Pharmaceuticals (USA) Inc.'s NDC 68382-792.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Zydus Pharmaceuticals (USA) Inc. names for other drugs.
Repackaging site
- Proficient Rx LP, Thousand Oaks, CA, United States · repackages it and relabels it
Recalls
- Apr 25, 2019 · Class II · Zydus Pharmaceuticals USA Inc
Labeling; Label Mix-up; report received of one bottle labeled as Acyclovir Tablets USP 400 mg actually contained Carvedilol Tablets 6.25 mg
Lots: Z804517, Nov 30, 2020
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 ANDA204314
- On the market since
- Sep 10, 2014
- Package NDCs
63187-366-3063187-366-3563187-366-6063187-366-90- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2021
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?