01 1AMIFAMPRIDINE PHOSPHATE
02 7PERAMPANEL
03 1VAMOROLONE
01 9CATALYST PHARMS
01 2SUSPENSION;ORAL
02 7TABLET;ORAL
01 10.5MG/ML
02 110MG
03 112MG
04 12MG
05 140MG/ML
06 14MG
07 16MG
08 18MG
09 1EQ 10MG BASE
01 9USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : FIRDAPSE
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 2018-11-28
Application Number : 208078
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : FYCOMPA
Dosage Strength : 2MG
Packaging :
Approval Date : 2012-10-22
Application Number : 202834
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : FYCOMPA
Dosage Strength : 4MG
Packaging :
Approval Date : 2012-10-22
Application Number : 202834
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : FYCOMPA
Dosage Strength : 6MG
Packaging :
Approval Date : 2012-10-22
Application Number : 202834
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : FYCOMPA
Dosage Strength : 8MG
Packaging :
Approval Date : 2012-10-22
Application Number : 202834
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : FYCOMPA
Dosage Strength : 10MG
Packaging :
Approval Date : 2012-10-22
Application Number : 202834
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : FYCOMPA
Dosage Strength : 12MG
Packaging :
Approval Date : 2012-10-22
Application Number : 202834
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SUSPENSION;ORAL
Brand Name : FYCOMPA
Dosage Strength : 0.5MG/ML
Packaging :
Approval Date : 2016-04-29
Application Number : 208277
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SUSPENSION;ORAL
Brand Name : AGAMREE
Dosage Strength : 40MG/ML
Packaging :
Approval Date : 2023-10-26
Application Number : 215239
Regulatory Info : RX
Registration Country : USA
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