NDC 69117-0010-01 - Valacyclovir
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 69117-0010
- Requested NDC
- 69117-0010-01
- Package NDCs from labels
- 69117-0010-1, 69117-0010-2, 69117-0010-3, 69117-0010-01
- Manufacturer
- Yiling Pharmaceutical, Inc. | Yiling Pharmaceutical Ltd
- Effective date
- 2025-12-29
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Valacyclovir - Yiling Pharmaceutical, Inc. | Yiling Pharmaceutical Ltd | Yiling Pharmaceutical, Inc. | Yiling Pharmaceutical Ltd | 2025-12-29 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69117-0010-1 | Valacyclovir | 30 in 1 BOTTLE | TABLET | 30 | 9 | |
| 69117-0010-2 | Valacyclovir | 90 in 1 BOTTLE | TABLET | 90 | 9 | |
| 69117-0010-3 | Valacyclovir | 500 in 1 BOTTLE | TABLET | 500 | 9 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 69117-0010 | VALACYCLOVIR TABLET VALACYCLOVIR (VALACYCLOVIR HYDROCHLORIDE) TABLET [YILING PHARMACEUTICAL, INC.] | 8 | Current NDC, Legacy NDC, 3 package rows | 20250101_f3ee4017-a4fc-475d-a49b-b39168ec5966.zip |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.