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
- 76420-600_1cf37738-8be1-f5cf-e063-6394a90af194
- Product NDC
- 76420-600
- Form
- TABLET, FILM COATED
- Composition / generic term
- Valacyclovir Hydrochloride
- Labeler
- Asclemed USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20100524
- Source listing expiry
- 20261231
Source-listed ingredients
- VALACYCLOVIR HYDROCHLORIDE — 1 g/1
These values do not establish equivalence or a dose recommendation.
Packages
- 2 TABLET, FILM COATED in 1 BOTTLE (76420-600-02) · 76420-600-02
- 4 TABLET, FILM COATED in 1 BOTTLE (76420-600-04) · 76420-600-04
- 7 TABLET, FILM COATED in 1 BOTTLE (76420-600-07) · 76420-600-07
- 10 TABLET, FILM COATED in 1 BOTTLE (76420-600-10) · 76420-600-10
- 15 TABLET, FILM COATED in 1 BOTTLE (76420-600-15) · 76420-600-15
- 20 TABLET, FILM COATED in 1 BOTTLE (76420-600-20) · 76420-600-20
- 21 TABLET, FILM COATED in 1 BOTTLE (76420-600-21) · 76420-600-21
- 30 TABLET, FILM COATED in 1 BOTTLE (76420-600-30) · 76420-600-30
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 →