NDC 84670-014 – Mifepristone

Mifepristone 200 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC84670-014

Product details

Brand name
Mifepristone
Generic name
Mifepristone
Labeler
Evita Solutions LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA216616
Marketed since
July 29, 2026
Listing expires
December 31, 2027
Pharmacologic class
Progestin Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Mifepristone →

Package NDC codes (1)

Package NDCDescriptionSince
84670-014-011 TABLET in 1 BLISTER PACK (84670-014-01)Jul 29, 2026

Other Mifepristone products