Mycophenolic Acid

Product NDC
0093-7031
11-digit product format
000937031
Labeler code
0093
Product ID
0093-7031_510747d8-e048-4d8b-a0f7-00e3723c1738
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Mycophenolic Acid
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Labeler
Teva Pharmaceuticals USA, Inc.
Application
ANDA202720
Marketing category
ANDA
Marketing start
2019-08-15
Marketing end
2020-09-30
Substance
MYCOPHENOLATE SODIUM
Active strength
180 mg/1
Pharmacologic classes
Antimetabolite Immunosuppressant [EPC]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0093-7031-89EA - Each0093-7031e8c07e3e-1d96-4e51-bf9b-c510f3a0b6b512019-09-05