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
- 68788-8724_9ffeaf80-77c0-43c2-9acb-469d537c184a
- Product NDC
- 68788-8724
- Form
- TABLET
- Composition / generic term
- Acyclovir
- Labeler
- Preferred Pharmaceuticals Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240816
- Source listing expiry
- 20271231
Source-listed ingredients
- ACYCLOVIR — 400 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (68788-8724-1) · 68788-8724-1
- 21 TABLET in 1 BOTTLE (68788-8724-2) · 68788-8724-2
- 30 TABLET in 1 BOTTLE (68788-8724-3) · 68788-8724-3
- 40 TABLET in 1 BOTTLE (68788-8724-4) · 68788-8724-4
- 50 TABLET in 1 BOTTLE (68788-8724-5) · 68788-8724-5
- 35 TABLET in 1 BOTTLE (68788-8724-8) · 68788-8724-8
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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