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
- 61442-112_209d3251-8d40-86dc-e063-6394a90a3492
- Product NDC
- 61442-112
- Form
- TABLET
- Composition / generic term
- Acyclovir
- Labeler
- Carlsbad Technology, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20091022
- Source listing expiry
- 20261231
Source-listed ingredients
- ACYCLOVIR — 400 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 24 BOTTLE, PLASTIC in 1 BOX (61442-112-01) / 100 TABLET in 1 BOTTLE, PLASTIC · 61442-112-01
- 12 BOTTLE, PLASTIC in 1 BOX (61442-112-05) / 500 TABLET in 1 BOTTLE, PLASTIC · 61442-112-05
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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