United States · FDA National Drug Code directory

EVRYSDI

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
50242-175_a0597961-b4b9-47ec-961a-919fa9ffba95
Product NDC
50242-175
Form
POWDER, FOR SOLUTION
Composition / generic term
Risdiplam
Labeler
Genentech, Inc.
Marketing category
NDA
Marketing start / end (source format)
20200807
Source listing expiry
20271231

Source-listed ingredients

  • RISDIPLAM — .75 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE, GLASS in 1 CARTON (50242-175-07) / 80 mL in 1 BOTTLE, GLASS · 50242-175-07

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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