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
31722-681_e87a8107-f6d9-5bf2-e053-2a95a90afc80
Product NDC
31722-681
Form
SUSPENSION
Composition / generic term
Acyclovir
Labeler
Camber Pharmaceuticals, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20220701
Source listing expiry
20261231

Source-listed ingredients

  • ACYCLOVIR — 200 mg/5mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 473 mL in 1 BOTTLE (31722-681-47) · 31722-681-47

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 →