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
- 71335-0708_58ea1068-9302-4edd-acfa-4f539aa58427
- Product NDC
- 71335-0708
- Form
- TABLET, FILM COATED
- Composition / generic term
- Valacyclovir Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20100524
- Source listing expiry
- 20271231
Source-listed ingredients
- VALACYCLOVIR HYDROCHLORIDE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-0708-0) · 71335-0708-0
- 15 TABLET, FILM COATED in 1 BOTTLE (71335-0708-1) · 71335-0708-1
- 10 TABLET, FILM COATED in 1 BOTTLE (71335-0708-2) · 71335-0708-2
- 4 TABLET, FILM COATED in 1 BOTTLE (71335-0708-3) · 71335-0708-3
- 7 TABLET, FILM COATED in 1 BOTTLE (71335-0708-4) · 71335-0708-4
- 20 TABLET, FILM COATED in 1 BOTTLE (71335-0708-5) · 71335-0708-5
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-0708-6) · 71335-0708-6
- 8 TABLET, FILM COATED in 1 BOTTLE (71335-0708-7) · 71335-0708-7
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-0708-8) · 71335-0708-8
- 14 TABLET, FILM COATED in 1 BOTTLE (71335-0708-9) · 71335-0708-9
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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