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
- 68788-7575_9248c792-3664-4f8e-9d1d-3c4344deb9fc
- Product NDC
- 68788-7575
- Form
- TABLET
- Composition / generic term
- Acyclovir
- Labeler
- Preferred Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20131129
- Source listing expiry
- 20271231
Source-listed ingredients
- ACYCLOVIR — 800 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 21 TABLET in 1 BOTTLE (68788-7575-2) · 68788-7575-2
- 30 TABLET in 1 BOTTLE (68788-7575-3) · 68788-7575-3
- 40 TABLET in 1 BOTTLE (68788-7575-4) · 68788-7575-4
- 50 TABLET in 1 BOTTLE (68788-7575-5) · 68788-7575-5
- 60 TABLET in 1 BOTTLE (68788-7575-6) · 68788-7575-6
- 25 TABLET in 1 BOTTLE (68788-7575-7) · 68788-7575-7
- 35 TABLET in 1 BOTTLE (68788-7575-8) · 68788-7575-8
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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