01 1BENZYL ALCOHOL
02 1CEFIDEROCOL SULFATE TOSYLATE
03 2DORIPENEM
04 2Naldemedintosilat
05 1SULFAMETHOXAZOLE
06 2SULFAMETHOXAZOLE; TRIMETHOPRIM
07 4TACRINE HYDROCHLORIDE
08 1TRAMADOL HYDROCHLORIDE
01 3SHIONOGI
02 9SHIONOGI INC
03 2Shionogi B.V.
01 4CAPSULE;ORAL
02 2INJECTABLE;INTRAVENOUS
03 1LOTION;TOPICAL
04 1POWDER;INTRAVENOUS
05 1TABLET, ORALLY DISINTEGRATING;ORAL
06 3TABLET;ORAL
07 2Tablet, film-coated
01 2200 microg
02 1250MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
03 1400MG;80MG
04 15% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
05 1500MG
06 1500MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
07 150MG
08 1800MG;160MG
09 1EQ 10MG BASE
10 1EQ 1GM BASE/VIAL
11 1EQ 20MG BASE
12 1EQ 30MG BASE
13 1EQ 40MG BASE
01 2Norway
02 12USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : LOTION;TOPICAL
Brand Name : ULESFIA
Dosage Strength : 5% **Federal Register ...
Packaging :
Approval Date : 2009-04-09
Application Number : 22129
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : POWDER;INTRAVENOUS
Brand Name : FETROJA
Dosage Strength : EQ 1GM BASE/VIAL
Packaging :
Approval Date : 2019-11-14
Application Number : 209445
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INTRAVENOUS
Brand Name : DORIBAX
Dosage Strength : 500MG/VIAL **Federal R...
Packaging :
Approval Date : 2007-10-12
Application Number : 22106
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INTRAVENOUS
Brand Name : DORIBAX
Dosage Strength : 250MG/VIAL **Federal R...
Packaging :
Approval Date : 2010-10-05
Application Number : 22106
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info :
Registration Country : Norway
Dosage Form : Tablet, film-coated
Brand Name : Rizmoic
Dosage Strength : 200 microg
Packaging : Blisterpakning 100item
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Dosage Form : Tablet, film-coated
Brand Name : Rizmoic
Dosage Strength : 200 microg
Packaging : Blisterpakning 30item
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : UROBAK
Dosage Strength : 500MG
Packaging :
Approval Date : 1982-01-01
Application Number : 87307
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
SULFAMETHOXAZOLE; TRIMETHOPRIM
Dosage Form : TABLET;ORAL
Brand Name : UROPLUS SS
Dosage Strength : 400MG;80MG
Packaging :
Approval Date : 1987-09-28
Application Number : 71815
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
SULFAMETHOXAZOLE; TRIMETHOPRIM
Dosage Form : TABLET;ORAL
Brand Name : UROPLUS DS
Dosage Strength : 800MG;160MG
Packaging :
Approval Date : 1987-09-28
Application Number : 71816
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : COGNEX
Dosage Strength : EQ 20MG BASE
Packaging :
Approval Date : 1993-09-09
Application Number : 20070
Regulatory Info : DISCN
Registration Country : USA
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