NDC 76346-654 – Mifepristone

Mifepristone 300 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC76346-654

Product details

Brand name
Mifepristone
Generic name
Mifepristone
Labeler
Corcept Therapeutics Incorporated
Dosage form
Tablet
Route
Oral
Marketing category
NDA · NDA202107
Marketed since
May 28, 2024
Listing expires
December 31, 2026
Pharmacologic class
Progestin Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Mifepristone →

Package NDC codes (1)

Package NDCDescriptionSince
76346-654-03280 TABLET in 1 BOTTLE (76346-654-03)May 28, 2024

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