01 1ACETAMINOPHEN; BUTALBITAL; CAFFEINE
02 1ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE
03 1CIPROFLOXACIN HYDROCHLORIDE
04 1DEXAMETHASONE
05 4FENOPROFEN CALCIUM
06 1VORAPAXAR SULFATE
01 9KEY THERAP
01 5CAPSULE;ORAL
02 1SOLUTION/DROPS;OTIC
03 3TABLET;ORAL
01 11.5MG
02 1300MG;50MG;40MG
03 1320.5MG;30MG;16MG
04 1EQ 0.2% BASE
05 1EQ 2.08MG BASE
06 1EQ 200MG BASE
07 1EQ 300MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
08 1EQ 400MG BASE
09 1EQ 600MG BASE
01 9USA
Regulatory Info : DISCN
Registration Country : USA
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Dosage Form : CAPSULE;ORAL
Brand Name : BUTALBITAL, ACETAMINOPHEN...
Dosage Strength : 300MG;50MG;40MG
Packaging :
Approval Date : 2017-08-04
Application Number : 206615
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE
Dosage Form : CAPSULE;ORAL
Brand Name : TREZIX
Dosage Strength : 320.5MG;30MG;16MG
Packaging :
Approval Date : 2014-11-26
Application Number : 204785
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION/DROPS;OTIC
Brand Name : CETRAXAL
Dosage Strength : EQ 0.2% BASE
Packaging :
Approval Date : 2009-05-01
Application Number : 21918
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : DEXAMETHASONE
Dosage Strength : 1.5MG
Packaging :
Approval Date : 1983-04-28
Application Number : 88237
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : NALFON
Dosage Strength : EQ 300MG BASE **Federa...
Packaging :
Approval Date : 1982-01-01
Application Number : 17604
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : NALFON
Dosage Strength : EQ 200MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 17604
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : NALFON
Dosage Strength : EQ 400MG BASE
Packaging :
Approval Date : 2009-07-21
Application Number : 17604
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : FENOPROFEN CALCIUM
Dosage Strength : EQ 600MG BASE
Packaging :
Approval Date : 1988-08-17
Application Number : 72267
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ZONTIVITY
Dosage Strength : EQ 2.08MG BASE
Packaging :
Approval Date : 2014-05-08
Application Number : 204886
Regulatory Info : DISCN
Registration Country : USA
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