
Reset all filters
01 2Accord healthcare
02 2Alkem Laboratories
03 2American Massage Therapy Association
04 4Apotex Inc
05 2Ascend Labs
06 2Aurobindo Pharma Limited
07 4Biocon
08 2Concord Biotech
09 2FOSUN WANBANG
10 2JAMP PHARMA
11 2MARCAN PHARMACEUTICALS INC
12 4Novartis Pharmaceuticals Corporation
13 2RK Pharma
14 2TWi Pharmaceuticals
15 4Teva Pharmaceutical Industries
16 2World Medicine
Reset all filters
01 2GASTRO
02 2TAB
03 1TABLET
04 8TABLET (ENTERIC-COATED)
05 26TABLET, DELAYED RELEASE;ORAL
06 1Blank
Reset all filters
01 2DISCN
02 2Generic
03 8Prescription
04 24RX
05 4Blank
Reset all filters
01 2APO-MYCOPHENOLIC ACID
02 2Axympa
03 2JAMP MYCOPHENOLIC ACID
04 2MAR-MYCOPHENOLIC ACID
05 1MIKA
06 24MYCOPHENOLIC SODIUM
07 4MYFORTIC
08 1Transwel 180
09 1Transwel 360
10 1Blank
Reset all filters
01 8Canada
02 2South Africa
03 2Sweden
04 2Turkey
05 26USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MYCOPHENOLIC SODIUM
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : EQ 180MG BASE
Packaging :
Approval Date : 2017-08-23
Application Number : 202555
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MYCOPHENOLIC SODIUM
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : EQ 360MG BASE
Packaging :
Approval Date : 2017-08-23
Application Number : 202555
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MYCOPHENOLIC SODIUM
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : EQ 180MG BASE
Packaging :
Approval Date : 2021-09-23
Application Number : 208315
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MYCOPHENOLIC SODIUM
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : EQ 360MG BASE
Packaging :
Approval Date : 2021-09-23
Application Number : 208315
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MYCOPHENOLIC SODIUM
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : EQ 180MG BASE
Packaging :
Approval Date : 2021-02-10
Application Number : 214376
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MYCOPHENOLIC SODIUM
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : EQ 360MG BASE
Packaging :
Approval Date : 2021-02-10
Application Number : 214376
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MYCOPHENOLIC SODIUM
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : EQ 180MG BASE
Packaging :
Approval Date : 2012-08-21
Application Number : 91558
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MYCOPHENOLIC SODIUM
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : EQ 360MG BASE
Packaging :
Approval Date : 2014-08-19
Application Number : 91558
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MYCOPHENOLIC SODIUM
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : EQ 180MG BASE
Packaging :
Approval Date : 2021-11-29
Application Number : 214630
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MYCOPHENOLIC SODIUM
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : EQ 360MG BASE
Packaging :
Approval Date : 2021-11-29
Application Number : 214630
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MYCOPHENOLIC SODIUM
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : EQ 180MG BASE
Packaging :
Approval Date : 2019-12-13
Application Number : 211173
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MYCOPHENOLIC SODIUM
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : EQ 360MG BASE
Packaging :
Approval Date : 2019-12-13
Application Number : 211173
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MYFORTIC
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : EQ 180MG BASE
Packaging :
Approval Date : 2004-02-27
Application Number : 50791
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MYFORTIC
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : EQ 360MG BASE
Packaging :
Approval Date : 2004-02-27
Application Number : 50791
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MYCOPHENOLIC SODIUM
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : EQ 360MG BASE
Packaging :
Approval Date : 2014-01-08
Application Number : 91248
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MYCOPHENOLIC SODIUM
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : EQ 180MG BASE
Packaging :
Approval Date : 2014-01-08
Application Number : 91248
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : MYCOPHENOLIC SODIUM
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : EQ 180MG BASE
Packaging :
Approval Date : 2014-10-30
Application Number : 202720
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : MYCOPHENOLIC SODIUM
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : EQ 360MG BASE
Packaging :
Approval Date : 2014-10-30
Application Number : 202720
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MYCOPHENOLIC SODIUM
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : EQ 180MG BASE
Packaging :
Approval Date : 2021-11-03
Application Number : 214289
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MYCOPHENOLIC SODIUM
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : EQ 360MG BASE
Packaging :
Approval Date : 2021-11-03
Application Number : 214289
Regulatory Info : RX
Registration Country : USA