United States · FDA National Drug Code directory
Valacyclovir
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 69117-0011_47237b45-ce93-292b-e063-6394a90a1ab5
- Product NDC
- 69117-0011
- Form
- TABLET
- Composition / generic term
- Valacyclovir Hydrochloride
- Labeler
- Yiling Pharmaceutical, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20181001
- Source listing expiry
- 20261231
Source-listed ingredients
- VALACYCLOVIR HYDROCHLORIDE — 1 g/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (69117-0011-1) · 69117-0011-1
- 90 TABLET in 1 BOTTLE (69117-0011-2) · 69117-0011-2
- 500 TABLET in 1 BOTTLE (69117-0011-3) · 69117-0011-3
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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