NDC 59651-638 – Mycophenolate Mofetil

Mycophenolate Mofetil 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC59651-638

Product details

Brand name
Mycophenolate Mofetil
Generic name
Mycophenolate Mofetil
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA217937
Marketed since
February 20, 2024
Listing expires
December 31, 2026
Pharmacologic class
Antimetabolite Immunosuppressant

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
59651-638-01100 TABLET, FILM COATED in 1 BOTTLE (59651-638-01)Feb 20, 2024
59651-638-05500 TABLET, FILM COATED in 1 BOTTLE (59651-638-05)Feb 20, 2024

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