NDC 71904-300 – Opfolda

Miglustat 65 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71904-300

Product details

Brand name
Opfolda
Generic name
Miglustat
Labeler
AMICUS THERAPEUTICS US, LLC
Dosage form
Capsule
Route
Oral
Marketing category
NDA · NDA215211
Marketed since
October 11, 2023
Listing expires
December 31, 2026
Pharmacologic class
Enzyme Stabilizer; Glucosylceramide Synthase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Opfolda →

Package NDC codes (3)

Package NDCDescriptionSince
71904-300-014 BOTTLE, PLASTIC in 1 BOTTLE, PLASTIC (71904-300-01) / 1 CAPSULE in 1 BOTTLE, PLASTICOct 11, 2023
71904-300-0224 BOTTLE, PLASTIC in 1 BOTTLE, PLASTIC (71904-300-02) / 1 CAPSULE in 1 BOTTLE, PLASTICOct 11, 2023
71904-300-03100 BOTTLE, PLASTIC in 1 BOTTLE, PLASTIC (71904-300-03) / 1 CAPSULE in 1 BOTTLE, PLASTICOct 11, 2023