NDC 0591-4390 – Mifepristone

Mifepristone 300 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC0591-4390

Product details

Brand name
Mifepristone
Generic name
Mifepristone
Labeler
Actavis Pharma, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA211436
Marketed since
January 19, 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
0591-4390-9628 TABLET, FILM COATED in 1 BOTTLE (0591-4390-96)Jan 19, 2024

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