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
- 71335-0695_b4baef46-4b41-48c0-98c3-27068950a018
- Product NDC
- 71335-0695
- Form
- TABLET
- Composition / generic term
- Acyclovir
- Labeler
- Bryant Ranch Prepack
- 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
- 500 TABLET in 1 BOTTLE (71335-0695-0) · 71335-0695-0
- 25 TABLET in 1 BOTTLE (71335-0695-1) · 71335-0695-1
- 35 TABLET in 1 BOTTLE (71335-0695-2) · 71335-0695-2
- 30 TABLET in 1 BOTTLE (71335-0695-3) · 71335-0695-3
- 60 TABLET in 1 BOTTLE (71335-0695-4) · 71335-0695-4
- 50 TABLET in 1 BOTTLE (71335-0695-5) · 71335-0695-5
- 10 TABLET in 1 BOTTLE (71335-0695-6) · 71335-0695-6
- 40 TABLET in 1 BOTTLE (71335-0695-7) · 71335-0695-7
- 21 TABLET in 1 BOTTLE (71335-0695-8) · 71335-0695-8
- 90 TABLET in 1 BOTTLE (71335-0695-9) · 71335-0695-9
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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