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
- 59746-325_40211dd2-c21e-45a4-a8d4-04febf925f52
- Product NDC
- 59746-325
- Form
- TABLET, FILM COATED
- Composition / generic term
- valacyclovir hydrochloride
- Labeler
- Jubilant Cadista Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20120405
- Source listing expiry
- 20261231
Source-listed ingredients
- VALACYCLOVIR HYDROCHLORIDE — 1 g/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (59746-325-01) · 59746-325-01
- 10 TABLET, FILM COATED in 1 BOTTLE (59746-325-10) · 59746-325-10
- 30 TABLET, FILM COATED in 1 BOTTLE (59746-325-30) · 59746-325-30
- 250 TABLET, FILM COATED in 1 BOTTLE (59746-325-37) · 59746-325-37
- 300 TABLET, FILM COATED in 1 BOTTLE (59746-325-47) · 59746-325-47
- 90 TABLET, FILM COATED in 1 BOTTLE (59746-325-90) · 59746-325-90
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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