NDC 68071-3767 – Mycophenolate mofetil

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

Human Prescription Drug

Product NDC68071-3767

Product details

Brand name
Mycophenolate mofetil
Generic name
Mycophenolate mofetil
Labeler
NuCare Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090456
Marketed since
November 6, 2010
Listing expires
December 31, 2026
Pharmacologic class
Antimetabolite Immunosuppressant

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
68071-3767-660 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3767-6)Jan 13, 2025

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