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
- 68788-7587_c347cba6-fba8-4c16-9584-c79d6c2a8179
- Product NDC
- 68788-7587
- Form
- TABLET, FILM COATED
- Composition / generic term
- Valacyclovir
- Labeler
- Preferred Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150525
- Source listing expiry
- 20261231
Source-listed ingredients
- VALACYCLOVIR HYDROCHLORIDE — 1 g/1
These values do not establish equivalence or a dose recommendation.
Packages
- 6 TABLET, FILM COATED in 1 BOTTLE (68788-7587-0) · 68788-7587-0
- 10 TABLET, FILM COATED in 1 BOTTLE (68788-7587-1) · 68788-7587-1
- 20 TABLET, FILM COATED in 1 BOTTLE (68788-7587-2) · 68788-7587-2
- 30 TABLET, FILM COATED in 1 BOTTLE (68788-7587-3) · 68788-7587-3
- 4 TABLET, FILM COATED in 1 BOTTLE (68788-7587-4) · 68788-7587-4
- 15 TABLET, FILM COATED in 1 BOTTLE (68788-7587-5) · 68788-7587-5
- 21 TABLET, FILM COATED in 1 BOTTLE (68788-7587-7) · 68788-7587-7
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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