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
- 70518-0541_552b4868-06bd-cb7c-e063-6294a90aa6fb
- Product NDC
- 70518-0541
- Form
- TABLET, FILM COATED
- Composition / generic term
- valacyclovir hydrochloride
- Labeler
- REMEDYREPACK INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170515
- Source listing expiry
- 20271231
Source-listed ingredients
- VALACYCLOVIR HYDROCHLORIDE — 1 g/1
These values do not establish equivalence or a dose recommendation.
Packages
- 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0541-1) · 70518-0541-1
- 5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0541-2) · 70518-0541-2
- 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0541-3) · 70518-0541-3
- 4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0541-4) · 70518-0541-4
- 5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0541-5) · 70518-0541-5
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 →