Yiling Pharmaceutical Ltd
Shijiazhuang, China · makes it
Serious problems, FDA action Last FDA inspection Oct 11, 2024. 2 inspections on record, 1 with serious problems.
NDC 23155-962
Acyclovir 200 mg capsule
On the label: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc..
Where it's made
Product details
- Generic drug
- Acyclovir: see every company that makes it
- Form
- capsule, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA212173
- On the market since
- Mar 25, 2026
- Package NDCs
23155-962-0123155-962-05- Official label
- DailyMed (National Library of Medicine), updated Mar 25, 2026
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