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
- 72162-1724_a45392d2-5725-47dc-a6c5-50a98f93031a
- Product NDC
- 72162-1724
- Form
- TABLET
- Composition / generic term
- acyclovir
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20060313 / 20261231
Source-listed ingredients
- ACYCLOVIR — 800 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 40 TABLET in 1 BOTTLE (72162-1724-0) · 72162-1724-0
- 21 TABLET in 1 BOTTLE (72162-1724-1) · 72162-1724-1
- 25 TABLET in 1 BOTTLE (72162-1724-2) · 72162-1724-2
- 30 TABLET in 1 BOTTLE (72162-1724-3) · 72162-1724-3
- 35 TABLET in 1 BOTTLE (72162-1724-4) · 72162-1724-4
- 500 TABLET in 1 BOTTLE (72162-1724-5) · 72162-1724-5
- 60 TABLET in 1 BOTTLE (72162-1724-6) · 72162-1724-6
- 50 TABLET in 1 BOTTLE (72162-1724-7) · 72162-1724-7
- 10 TABLET in 1 BOTTLE (72162-1724-8) · 72162-1724-8
- 90 TABLET in 1 BOTTLE (72162-1724-9) · 72162-1724-9
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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