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
- 68382-048_515388e8-636f-42f6-a39e-bb4fc7c2e7cb
- Product NDC
- 68382-048
- Form
- INJECTION, SOLUTION
- Composition / generic term
- ACYCLOVIR
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20181127
- Source listing expiry
- 20261231
Source-listed ingredients
- ACYCLOVIR SODIUM — 50 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL, SINGLE-USE in 1 CARTON (68382-048-10) / 10 mL in 1 VIAL, SINGLE-USE (68382-048-01) · 68382-048-10
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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