Mycophenolate Mofetil

Product NDC

68084-795

11-digit product format

680840795

Labeler code

68084

Product ID

68084-795_77fa20a9-f6e6-2f19-e053-2991aa0aa9c2

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Mycophenolate Mofetil

Dosage form

CAPSULE

Route

ORAL

Labeler

American Health Packaging

Application

ANDA065379

Marketing category

ANDA

Marketing start

2015-02-05

Marketing end

2020-03-31

Substance

MYCOPHENOLATE MOFETIL

Active strength

250 mg/1

Pharmacologic classes

Antimetabolite Immunosuppressant [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record