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
- 63304-904_536bdec7-e486-ae91-e063-6294a90a0ed7
- Product NDC
- 63304-904
- Form
- TABLET, FILM COATED
- Composition / generic term
- Valacyclovir
- Labeler
- SUN PHARMACEUTICAL INDUSTRIES, INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20201219
- 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 (63304-904-03) · 63304-904-03
- 500 TABLET, FILM COATED in 1 BOTTLE (63304-904-05) · 63304-904-05
- 100 BLISTER PACK in 1 CARTON (63304-904-77) / 1 TABLET, FILM COATED in 1 BLISTER PACK (63304-904-11) · 63304-904-77
- 90 TABLET, FILM COATED in 1 BOTTLE (63304-904-90) · 63304-904-90
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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