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
- 68788-8705_b4046250-4f62-4395-8cd0-cdd31edca208
- Product NDC
- 68788-8705
- Form
- TABLET
- Composition / generic term
- Valacyclovir
- Labeler
- Preferred Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240701
- Source listing expiry
- 20261231
Source-listed ingredients
- VALACYCLOVIR HYDROCHLORIDE — 1000 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 6 TABLET in 1 BOTTLE (68788-8705-0) · 68788-8705-0
- 10 TABLET in 1 BOTTLE (68788-8705-1) · 68788-8705-1
- 20 TABLET in 1 BOTTLE (68788-8705-2) · 68788-8705-2
- 30 TABLET in 1 BOTTLE (68788-8705-3) · 68788-8705-3
- 4 TABLET in 1 BOTTLE (68788-8705-4) · 68788-8705-4
- 15 TABLET in 1 BOTTLE (68788-8705-5) · 68788-8705-5
- 21 TABLET in 1 BOTTLE (68788-8705-7) · 68788-8705-7
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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