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
- 68462-746_091cd2ff-6773-415a-9529-4f8386512c41
- Product NDC
- 68462-746
- Form
- OINTMENT
- Composition / generic term
- acyclovir
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170731
- Source listing expiry
- 20271231
Source-listed ingredients
- ACYCLOVIR — 50 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (68462-746-17) / 15 g in 1 TUBE · 68462-746-17
- 1 TUBE in 1 CARTON (68462-746-35) / 30 g in 1 TUBE · 68462-746-35
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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