Zydus Lifesciences Limited
Ahmedabad, India · makes it and tests it
Problems found, fixed voluntarily Last FDA inspection Mar 24, 2023. 5 inspections on record.
NDC 53002-2452
acyclovir 200 mg capsule
On the label: RPK Pharmaceuticals, Inc..
It's a repackaged product: RPK Pharmaceuticals, Inc. rebottles it from Viona Pharmaceuticals Inc.'s NDC 72578-002.
Where the pills inside were made
Repackaging site
- RPK Pharmaceuticals, Inc., · repackages it and relabels it
Product details
- Generic drug
- Acyclovir: see every company that makes it
- Form
- capsule
- Strength
- 200 mg
- Approval
- ANDA ANDA204313
- On the market since
- Aug 23, 2019
- Package NDCs
53002-2452-153002-2452-2- Official label
- DailyMed (National Library of Medicine), updated Aug 7, 2023
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