NDC 60687-438 – Mycophenolate mofetil

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

Human Prescription Drug

Product NDC60687-438

Product details

Brand name
Mycophenolate mofetil
Generic name
Mycophenolate Mofetil
Labeler
American Health Packaging
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090456
Marketed since
June 14, 2019
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
60687-438-01100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-438-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-438-11)Jun 14, 2019

Other Mycophenolate Mofetil products