United States · FDA National Drug Code directory

KISQALI

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
0078-0867_9466e642-f230-43f3-b78e-5a432fa040ee
Product NDC
0078-0867
Form
TABLET, FILM COATED
Composition / generic term
ribociclib
Labeler
Novartis Pharmaceuticals Corporation
Marketing category
NDA
Marketing start / end (source format)
20170313
Source listing expiry
20271231

Source-listed ingredients

  • RIBOCICLIB SUCCINATE — 200 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 3 BLISTER PACK in 1 CARTON (0078-0867-42) / 14 TABLET, FILM COATED in 1 BLISTER PACK (0078-0867-14) · 0078-0867-42

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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