NDC 0054-0166 – Mycophenolate Mofetil

Mycophenolate Mofetil 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC0054-0166

Product details

Brand name
Mycophenolate Mofetil
Generic name
Mycophenolate Mofetil
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA065413
Marketed since
July 29, 2008
Marketing end
November 30, 2026
Pharmacologic class
Antimetabolite Immunosuppressant

Active ingredients

Uses, dosage, side effects and warnings for Mycophenolate Mofetil →

Package NDC codes (2)

Package NDCDescriptionSince
0054-0166-25100 TABLET in 1 BOTTLE (0054-0166-25)Jul 29, 2008
0054-0166-29500 TABLET in 1 BOTTLE (0054-0166-29)Jul 29, 2008

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