NDC 67046-1487
acyclovir 800 mg tablet
On the label: Coupler LLC. It's repackaged: Coupler LLC 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
- Coupler LLC, West Chester, PA, United States · repackages 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
- Jan 29, 2025
- Package NDCs
67046-1487-3- Official label
- DailyMed (National Library of Medicine), updated Jan 29, 2025
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