Valacyclovir HCl Tablets — Class II drug recall D-323-2014
Terminated recall by American Health Packaging, reported 2013-12-11, distributed nationwide. Subpotent
| Recall number | D-323-2014 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | American Health Packaging, Columbus, OH, United States |
| Recall initiated | 2013-08-02 |
| Classified | 2013-12-05 |
| Reported by FDA | 2013-12-11 |
| Terminated | 2015-06-26 |
| Distributed | Nationwide (US) |
| Quantity | 1,536 cartons |
| Reason classes | potency |
| NDC | 68084-0633-01, 68084-0633-11 |
| Lot numbers | 130007 |
| Expiration dates | 2014-01-31 |
Product
Valacyclovir HCl Tablets, 500 mg, 100 tablets (10x10) blister cards, Rx only, Packaged and Distributed by: American Health Packaging, Columbus, OH NDC 68084-633-01
Reason for recall
Subpotent
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-323-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.