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
- 33342-439_49a1e24d-5821-45a5-bf2f-0497f4fd3a1b
- Product NDC
- 33342-439
- Form
- OINTMENT
- Composition / generic term
- Acyclovir
- Labeler
- Macleods Pharmaceuticals Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180813
- Source listing expiry
- 20261231
Source-listed ingredients
- ACYCLOVIR — 50 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (33342-439-15) / 15 g in 1 TUBE · 33342-439-15
- 1 TUBE in 1 CARTON (33342-439-30) / 30 g in 1 TUBE · 33342-439-30
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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