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
- 51655-300_48eadee3-c054-1e41-e063-6294a90a6a66
- Product NDC
- 51655-300
- Form
- TABLET
- Composition / generic term
- Acyclovir
- Labeler
- Northwind Health Company, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20141022
- Source listing expiry
- 20271231
Source-listed ingredients
- ACYCLOVIR — 400 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 25 TABLET in 1 BOTTLE, DISPENSING (51655-300-23) · 51655-300-23
- 90 TABLET in 1 BOTTLE, PLASTIC (51655-300-26) · 51655-300-26
- 35 TABLET in 1 BOTTLE, PLASTIC (51655-300-35) · 51655-300-35
- 60 TABLET in 1 BOTTLE, PLASTIC (51655-300-50) · 51655-300-50
- 30 TABLET in 1 BOTTLE, DISPENSING (51655-300-52) · 51655-300-52
- 15 TABLET in 1 BOTTLE, PLASTIC (51655-300-54) · 51655-300-54
- 14 TABLET in 1 BOTTLE, PLASTIC (51655-300-84) · 51655-300-84
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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