United States · FDA National Drug Code directory
Valacyclovir Hydrochloride
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
- 70518-3359_5865bc8c-e7b6-47b4-e063-6394a90ad710
- Product NDC
- 70518-3359
- Form
- TABLET, FILM COATED
- Composition / generic term
- Valacyclovir Hydrochloride
- Labeler
- REMEDYREPACK INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220207
- Source listing expiry
- 20271231
Source-listed ingredients
- VALACYCLOVIR HYDROCHLORIDE — 1 g/1
These values do not establish equivalence or a dose recommendation.
Packages
- 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3359-1) · 70518-3359-1
- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3359-2) · 70518-3359-2
- 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3359-3) · 70518-3359-3
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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