United States · FDA National Drug Code directory

DAWNZERA

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
71860-103_3f909bfc-3281-a444-e063-6294a90a221f
Product NDC
71860-103
Form
INJECTION, SOLUTION
Composition / generic term
donidalorsen
Labeler
Ionis Pharmaceuticals Inc.
Marketing category
NDA
Marketing start / end (source format)
20250821
Source listing expiry
20261231

Source-listed ingredients

  • DONIDALORSEN SODIUM — 80 mg/.8mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 SYRINGE, GLASS in 1 CARTON (71860-103-01) / .8 mL in 1 SYRINGE, GLASS · 71860-103-01

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.

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