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
- 71335-0323_e20bedec-0eb8-4d24-9148-a3ece431dcba
- Product NDC
- 71335-0323
- 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 — 400 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 120 TABLET in 1 BOTTLE (71335-0323-0) · 71335-0323-0
- 20 TABLET in 1 BOTTLE (71335-0323-1) · 71335-0323-1
- 28 TABLET in 1 BOTTLE (71335-0323-2) · 71335-0323-2
- 30 TABLET in 1 BOTTLE (71335-0323-3) · 71335-0323-3
- 50 TABLET in 1 BOTTLE (71335-0323-4) · 71335-0323-4
- 15 TABLET in 1 BOTTLE (71335-0323-5) · 71335-0323-5
- 60 TABLET in 1 BOTTLE (71335-0323-6) · 71335-0323-6
- 25 TABLET in 1 BOTTLE (71335-0323-7) · 71335-0323-7
- 10 TABLET in 1 BOTTLE (71335-0323-8) · 71335-0323-8
- 40 TABLET in 1 BOTTLE (71335-0323-9) · 71335-0323-9
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →