United States · FDA National Drug Code directory
Acyclovir
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
- 54348-627_ea937906-dba1-207f-e053-2a95a90a111e
- Product NDC
- 54348-627
- Form
- TABLET
- Composition / generic term
- Acyclovir
- Labeler
- PharmPak, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20131129
- Source listing expiry
- 20261231
Source-listed ingredients
- ACYCLOVIR — 400 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 BOX (54348-627-10) / 10 TABLET in 1 BOTTLE · 54348-627-10
- 1 BOTTLE in 1 BOX (54348-627-15) / 15 TABLET in 1 BOTTLE · 54348-627-15
- 1 BOTTLE in 1 BOX (54348-627-20) / 20 TABLET in 1 BOTTLE · 54348-627-20
- 1 BOTTLE in 1 BOX (54348-627-21) / 21 TABLET in 1 BOTTLE · 54348-627-21
- 1 BOTTLE in 1 BOX (54348-627-25) / 25 TABLET in 1 BOTTLE · 54348-627-25
- 1 BOTTLE in 1 BOX (54348-627-30) / 30 TABLET in 1 BOTTLE · 54348-627-30
- 1 BOTTLE in 1 BOX (54348-627-60) / 60 TABLET in 1 BOTTLE · 54348-627-60
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 →