United States · FDA National Drug Code directory

Zydelig

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
61958-1701_ca3e7112-6dfe-403f-af6f-a0051e77d125
Product NDC
61958-1701
Form
TABLET, FILM COATED
Composition / generic term
idelalisib
Labeler
Gilead Sciences, Inc.
Marketing category
NDA
Marketing start / end (source format)
20140723
Source listing expiry
20261231

Source-listed ingredients

  • IDELALISIB — 100 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (61958-1701-1) · 61958-1701-1

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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Zydelig — United States | Molindra Medicines