NDC 23155-836 – Mycophenolate mofetil

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

Human Prescription Drug

Product NDC23155-836

Product details

Brand name
Mycophenolate mofetil
Generic name
Mycophenolate mofetil
Labeler
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090456
Marketed since
October 15, 2022
Marketing end
May 31, 2028
Pharmacologic class
Antimetabolite Immunosuppressant

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
23155-836-01100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (23155-836-01)Oct 15, 2022
23155-836-05500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (23155-836-05)Oct 15, 2022

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