11 Jun 2025
// FDA
03 Feb 2025
// FDA
21 Aug 2024
// FDA
Latest Content by PharmaCompass
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01 6BREXPIPRAZOLE
02 2PRUCALOPRIDE SUCCINATE
03 2SAFINAMIDE MESYLATE
04 1SAPROPTERIN DIHYDROCHLORIDE
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01 11ZENARA
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01 11TABLET;ORAL
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01 10.25MG
02 10.5MG
03 1100MG
04 11MG
05 12MG
06 13MG
07 14MG
08 1EQ 100MG BASE
09 1EQ 1MG BASE
10 1EQ 2MG BASE
11 1EQ 50MG BASE
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01 11USA
Regulatory Info :
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BREXPIPRAZOLE
Dosage Strength : 0.25MG
Packaging :
Approval Date :
Application Number : 213477
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BREXPIPRAZOLE
Dosage Strength : 0.5MG
Packaging :
Approval Date :
Application Number : 213477
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BREXPIPRAZOLE
Dosage Strength : 1MG
Packaging :
Approval Date :
Application Number : 213477
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BREXPIPRAZOLE
Dosage Strength : 2MG
Packaging :
Approval Date :
Application Number : 213477
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BREXPIPRAZOLE
Dosage Strength : 3MG
Packaging :
Approval Date :
Application Number : 213477
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BREXPIPRAZOLE
Dosage Strength : 4MG
Packaging :
Approval Date :
Application Number : 213477
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : PRUCALOPRIDE SUCCINATE
Dosage Strength : EQ 1MG BASE
Packaging :
Approval Date :
Application Number : 218795
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : PRUCALOPRIDE SUCCINATE
Dosage Strength : EQ 2MG BASE
Packaging :
Approval Date :
Application Number : 218795
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : SAFINAMIDE MESYLATE
Dosage Strength : EQ 50MG BASE
Packaging :
Approval Date :
Application Number : 215913
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : SAFINAMIDE MESYLATE
Dosage Strength : EQ 100MG BASE
Packaging :
Approval Date :
Application Number : 215913
Regulatory Info :
Registration Country : USA