NDC 0781-5175 – Mycophenolate Mofetil

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

Human Prescription Drug

Product NDC0781-5175

Product details

Brand name
Mycophenolate Mofetil
Generic name
Mycophenolate Mofetil
Labeler
Sandoz Inc
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA065451
Marketed since
October 15, 2008
Listing expires
December 31, 2026
Pharmacologic class
Antimetabolite Immunosuppressant

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
0781-5175-01100 TABLET, FILM COATED in 1 BOTTLE (0781-5175-01)Oct 15, 2008
0781-5175-05500 TABLET, FILM COATED in 1 BOTTLE (0781-5175-05)Oct 15, 2008
0781-5175-101000 TABLET, FILM COATED in 1 BOTTLE (0781-5175-10)Oct 15, 2008

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