mycophenolate mofetil

Product NDC

0093-7477

11-digit product format

000937477

Labeler code

0093

Product ID

0093-7477_3ce9d23f-834c-4184-8e42-9bd738905e76

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

mycophenolate mofetil

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Teva Pharmaceuticals USA, Inc.

Application

ANDA065457

Marketing category

ANDA

Marketing start

2009-05-05

Marketing end

2019-10-31

Substance

MYCOPHENOLATE MOFETIL

Active strength

500 mg/1

Pharmacologic classes

Antimetabolite Immunosuppressant [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record