01 4CLONIDINE HYDROCHLORIDE
02 4PREDNISOLONE SODIUM PHOSPHATE
01 8CONCORDIA PHARMS INC
01 1SOLUTION;ORAL
02 4TABLET, EXTENDED RELEASE;ORAL
03 3TABLET, ORALLY DISINTEGRATING;ORAL
01 10.1MG
02 10.1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
03 20.2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
04 1EQ 10MG BASE
05 1EQ 15MG BASE
06 1EQ 15MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
07 1EQ 30MG BASE
01 8USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET, EXTENDED RELEASE...
Brand Name : JENLOGA
Dosage Strength : 0.1MG **Federal Regist...
Packaging :
Approval Date : 2009-09-30
Application Number : 22331
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET, EXTENDED RELEASE...
Brand Name : JENLOGA
Dosage Strength : 0.2MG **Federal Regist...
Packaging :
Approval Date : 2010-05-25
Application Number : 22331
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET, EXTENDED RELEASE...
Brand Name : KAPVAY
Dosage Strength : 0.1MG
Packaging :
Approval Date : 2010-09-28
Application Number : 22331
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET, EXTENDED RELEASE...
Brand Name : KAPVAY
Dosage Strength : 0.2MG **Federal Regist...
Packaging :
Approval Date : 2010-09-28
Application Number : 22331
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET, ORALLY DISINTEGR...
Brand Name : ORAPRED ODT
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 2006-06-01
Application Number : 21959
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET, ORALLY DISINTEGR...
Brand Name : ORAPRED ODT
Dosage Strength : EQ 15MG BASE
Packaging :
Approval Date : 2006-06-01
Application Number : 21959
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET, ORALLY DISINTEGR...
Brand Name : ORAPRED ODT
Dosage Strength : EQ 30MG BASE
Packaging :
Approval Date : 2006-06-01
Application Number : 21959
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : SOLUTION;ORAL
Brand Name : ORAPRED
Dosage Strength : EQ 15MG BASE/5ML **Fed...
Packaging :
Approval Date : 2000-12-14
Application Number : 75117
Regulatory Info : DISCN
Registration Country : USA
LOOKING FOR A SUPPLIER?