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
- 65862-448_aecf12c1-9094-48b6-8cb0-fcace52e191a
- Product NDC
- 65862-448
- Form
- TABLET, FILM COATED
- Composition / generic term
- Valacyclovir Hydrochloride
- Labeler
- Aurobindo Pharma Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20100524
- Source listing expiry
- 20261231
Source-listed ingredients
- VALACYCLOVIR HYDROCHLORIDE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (65862-448-01) · 65862-448-01
- 500 TABLET, FILM COATED in 1 BOTTLE (65862-448-05) · 65862-448-05
- 10 BLISTER PACK in 1 CARTON (65862-448-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK · 65862-448-10
- 30 TABLET, FILM COATED in 1 BOTTLE (65862-448-30) · 65862-448-30
- 3500 TABLET, FILM COATED in 1 BOTTLE (65862-448-35) · 65862-448-35
- 90 TABLET, FILM COATED in 1 BOTTLE (65862-448-90) · 65862-448-90
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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