NDC 72603-751 – Mycophenolate Mofetil

Mycophenolate Mofetil 200 mg/mL · Powder, For Suspension · Oral

Human Prescription Drug

Product NDC72603-751

Product details

Brand name
Mycophenolate Mofetil
Generic name
Mycophenolate mofetil
Labeler
NorthStar Rx LLC
Dosage form
Powder, For Suspension
Route
Oral
Marketing category
ANDA · ANDA218227
Marketed since
March 1, 2026
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
72603-751-011 BOTTLE in 1 CARTON (72603-751-01) / 225 mL in 1 BOTTLEMar 1, 2026

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