United States · FDA National Drug Code directory
Valacyclovir
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
- 31722-705_461ff6f2-7bf1-82fb-e063-6294a90acb06
- Product NDC
- 31722-705
- Form
- TABLET, FILM COATED
- Composition / generic term
- Valacyclovir
- Labeler
- Camber Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150525
- 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 (31722-705-01) · 31722-705-01
- 500 TABLET, FILM COATED in 1 BOTTLE (31722-705-05) · 31722-705-05
- 30 TABLET, FILM COATED in 1 BOTTLE (31722-705-30) · 31722-705-30
- 60 TABLET, FILM COATED in 1 BOTTLE (31722-705-60) · 31722-705-60
- 90 TABLET, FILM COATED in 1 BOTTLE (31722-705-90) · 31722-705-90
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →