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
- 43063-730_51a5c9d3-30dc-519b-e063-6394a90a1e07
- Product NDC
- 43063-730
- Form
- TABLET, FILM COATED
- Composition / generic term
- Valacyclovir Hydrochloride
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- 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
- 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-730-10) · 43063-730-10
- 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-730-14) · 43063-730-14
- 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-730-90) · 43063-730-90
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 →