01 3AMLODIPINE BESYLATE
02 2CLOPIDOGREL BISULFATE
03 2DARIFENACIN HYDROBROMIDE
04 2MEMANTINE HYDROCHLORIDE
01 9POLYGEN PHARMS
01 2TABLET, EXTENDED RELEASE;ORAL
02 7TABLET;ORAL
01 110MG
02 15MG
03 1EQ 10MG BASE
04 1EQ 15MG BASE
05 1EQ 2.5MG BASE
06 1EQ 300MG BASE
07 1EQ 5MG BASE
08 1EQ 7.5MG BASE
09 1EQ 75MG BASE
01 9USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : AMLODIPINE BESYLATE
Dosage Strength : EQ 2.5MG BASE
Packaging :
Approval Date : 2016-07-11
Application Number : 207821
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : AMLODIPINE BESYLATE
Dosage Strength : EQ 5MG BASE
Packaging :
Approval Date : 2016-07-11
Application Number : 207821
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : AMLODIPINE BESYLATE
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 2016-07-11
Application Number : 207821
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : CLOPIDOGREL BISULFATE
Dosage Strength : EQ 75MG BASE
Packaging :
Approval Date : 2020-07-17
Application Number : 213351
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : CLOPIDOGREL BISULFATE
Dosage Strength : EQ 300MG BASE
Packaging :
Approval Date : 2020-07-17
Application Number : 213351
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET, EXTENDED RELEASE...
Brand Name : DARIFENACIN HYDROBROMIDE
Dosage Strength : EQ 7.5MG BASE
Packaging :
Approval Date : 2020-01-06
Application Number : 211045
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET, EXTENDED RELEASE...
Brand Name : DARIFENACIN HYDROBROMIDE
Dosage Strength : EQ 15MG BASE
Packaging :
Approval Date : 2020-01-06
Application Number : 211045
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : MEMANTINE HYDROCHLORIDE
Dosage Strength : 5MG
Packaging :
Approval Date : 2020-12-11
Application Number : 210587
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : MEMANTINE HYDROCHLORIDE
Dosage Strength : 10MG
Packaging :
Approval Date : 2020-12-11
Application Number : 210587
Regulatory Info : RX
Registration Country : USA
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