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
- 66267-399_1fa6dc86-6637-c362-e063-6394a90a4c03
- Product NDC
- 66267-399
- Form
- TABLET
- Composition / generic term
- acyclovir
- Labeler
- NuCare Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140910
- Source listing expiry
- 20261231
Source-listed ingredients
- ACYCLOVIR — 800 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 15 TABLET in 1 BOTTLE (66267-399-15) · 66267-399-15
- 21 TABLET in 1 BOTTLE (66267-399-21) · 66267-399-21
- 25 TABLET in 1 BOTTLE (66267-399-25) · 66267-399-25
- 30 TABLET in 1 BOTTLE (66267-399-30) · 66267-399-30
- 35 TABLET in 1 BOTTLE (66267-399-35) · 66267-399-35
- 50 TABLET in 1 BOTTLE (66267-399-50) · 66267-399-50
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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