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
- 71335-9620_57a5f652-a53e-4092-b597-28ef1bb60f17
- Product NDC
- 71335-9620
- Form
- TABLET
- Composition / generic term
- Acyclovir
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200815
- Source listing expiry
- 20261231
Source-listed ingredients
- ACYCLOVIR — 400 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 120 TABLET in 1 BOTTLE (71335-9620-0) · 71335-9620-0
- 20 TABLET in 1 BOTTLE (71335-9620-1) · 71335-9620-1
- 28 TABLET in 1 BOTTLE (71335-9620-2) · 71335-9620-2
- 30 TABLET in 1 BOTTLE (71335-9620-3) · 71335-9620-3
- 50 TABLET in 1 BOTTLE (71335-9620-4) · 71335-9620-4
- 15 TABLET in 1 BOTTLE (71335-9620-5) · 71335-9620-5
- 60 TABLET in 1 BOTTLE (71335-9620-6) · 71335-9620-6
- 25 TABLET in 1 BOTTLE (71335-9620-7) · 71335-9620-7
- 10 TABLET in 1 BOTTLE (71335-9620-8) · 71335-9620-8
- 40 TABLET in 1 BOTTLE (71335-9620-9) · 71335-9620-9
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 →