United States · FDA National Drug Code directory

MIGLUSTAT

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
43975-310_589c114d-45f1-423a-8064-846060d968ce
Product NDC
43975-310
Form
CAPSULE
Composition / generic term
MIGLUSTAT
Labeler
ANI Pharmaceuticals, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20180417
Source listing expiry
20261231

Source-listed ingredients

  • MIGLUSTAT — 100 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 6 BLISTER PACK in 1 CARTON (43975-310-83) / 15 CAPSULE in 1 BLISTER PACK (43975-310-08) · 43975-310-83

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 →
MIGLUSTAT — United States | Molindra Medicines