United States · FDA National Drug Code directory

SUSTOL

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
47426-101_7b12942e-ba3d-4921-8418-34dc5a0cb35b
Product NDC
47426-101
Form
INJECTION
Composition / generic term
granisetron
Labeler
Heron Therapeutics, Inc.
Marketing category
NDA
Marketing start / end (source format)
20160809
Source listing expiry
20271231

Source-listed ingredients

  • GRANISETRON — 10 mg/.4mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 6 KIT in 1 CARTON (47426-101-06) / 1 SYRINGE, GLASS in 1 KIT / .4 mL in 1 SYRINGE, GLASS · 47426-101-06

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.

Browse United States records →