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
- 61442-114_209d3e94-5d8e-8799-e063-6394a90ab9d1
- Product NDC
- 61442-114
- Form
- CAPSULE
- Composition / generic term
- Acyclovir
- Labeler
- Carlsbad Technology, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170817
- Source listing expiry
- 20261231
Source-listed ingredients
- ACYCLOVIR — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 12 BOTTLE, PLASTIC in 1 BOX (61442-114-01) / 100 CAPSULE in 1 BOTTLE, PLASTIC · 61442-114-01
- 12 BOTTLE, PLASTIC in 1 BOX (61442-114-05) / 500 CAPSULE in 1 BOTTLE, PLASTIC · 61442-114-05
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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