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: 71205-056_7fadb9ce-34cc-4b19-9470-15e3a64d9c4f
Product NDC: 71205-056
Form: TABLET
Composition / generic term: Acyclovir
Labeler: Proficient Rx LP
Marketing category: ANDA
Marketing start / end (source format): 20091022
Source listing expiry: 20261231

Source-listed ingredients

ACYCLOVIR — 400 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

30 TABLET in 1 BOTTLE, PLASTIC (71205-056-30) · 71205-056-30
60 TABLET in 1 BOTTLE, PLASTIC (71205-056-60) · 71205-056-60
90 TABLET in 1 BOTTLE, PLASTIC (71205-056-90) · 71205-056-90

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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