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
- 49483-690_c715d9f2-9fe1-0bdd-e053-2a95a90aecf2
- Product NDC
- 49483-690
- Form
- TABLET
- Composition / generic term
- Valacyclovir Hydrochloride
- Labeler
- TIME CAP LABORATORIES, INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210714
- Source listing expiry
- 20261231
Source-listed ingredients
- VALACYCLOVIR HYDROCHLORIDE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (49483-690-03) · 49483-690-03
- 10 TABLET in 1 BLISTER PACK (49483-690-04) · 49483-690-04
- 42 TABLET in 1 BOTTLE (49483-690-41) · 49483-690-41
- 500 TABLET in 1 BOTTLE (49483-690-50) · 49483-690-50
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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