NDC 50268-558 – Mycophenolate Mofetil

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

Human Prescription Drug

Product NDC50268-558

Product details

Brand name
Mycophenolate Mofetil
Generic name
Mycophenolate Mofetil
Labeler
AvPAK
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA091249
Marketed since
May 15, 2023
Listing expires
December 31, 2027
Pharmacologic class
Antimetabolite Immunosuppressant

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
50268-558-1550 BLISTER PACK in 1 BOX (50268-558-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-558-11)May 15, 2023

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