NDC 71610-033 – Mycophenolate Mofetil

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

Human Prescription Drug

Product NDC71610-033

Product details

Brand name
Mycophenolate Mofetil
Generic name
Mycophenolate mofetil
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA065521
Marketed since
January 6, 2015
Listing expires
December 31, 2026
Pharmacologic class
Antimetabolite Immunosuppressant

Active ingredients

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

Package NDC codes (7)

Package NDCDescriptionSince
71610-033-5360 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-033-53)Jul 1, 2019
71610-033-6090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-033-60)Jul 1, 2019
71610-033-70120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-033-70)Jan 19, 2018
71610-033-80180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-033-80)Jul 1, 2019
71610-033-90240 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-033-90)Jul 1, 2019
71610-033-92270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-033-92)Jul 1, 2019
71610-033-98540 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-033-98)Jul 1, 2019

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