United States · FDA National Drug Code directory

dactinomycin

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
39822-2100_19853d49-64c6-f1cd-e063-6294a90a9c95
Product NDC
39822-2100
Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Composition / generic term
dactinomycin
Labeler
XGen Pharmaceuticals DJB, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20190731
Source listing expiry
20261231

Source-listed ingredients

  • DACTINOMYCIN — .5 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 VIAL, SINGLE-DOSE in 1 CARTON (39822-2100-2) / 1 mL in 1 VIAL, SINGLE-DOSE (39822-2100-1) · 39822-2100-2

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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