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01 2DELAFLOXACIN MEGLUMINE
02 4METOPROLOL SUCCINATE
03 2ORITAVANCIN DIPHOSPHATE
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01 2MELINTA
02 6MELINTA THERAP
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01 3POWDER;INTRAVENOUS
02 4TABLET, EXTENDED RELEASE;ORAL
03 1TABLET;ORAL
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01 1EQ 1.2GM BASE/VIAL
02 1EQ 100MG TARTRATE
03 1EQ 200MG TARTRATE
04 1EQ 25MG TARTRATE
05 1EQ 300MG BASE/VIAL
06 1EQ 400MG BASE/VIAL
07 1EQ 450MG BASE
08 1EQ 50MG TARTRATE
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01 8USA
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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BAXDELA
Dosage Strength : EQ 450MG BASE
Packaging :
Approval Date : 2017-06-19
Application Number : 208610
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : POWDER;INTRAVENOUS
Brand Name : BAXDELA
Dosage Strength : EQ 300MG BASE/VIAL
Packaging :
Approval Date : 2017-06-19
Application Number : 208611
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET, EXTENDED RELEASE...
Brand Name : TOPROL-XL
Dosage Strength : EQ 50MG TARTRATE
Packaging :
Approval Date : 1992-01-10
Application Number : 19962
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET, EXTENDED RELEASE...
Brand Name : TOPROL-XL
Dosage Strength : EQ 100MG TARTRATE
Packaging :
Approval Date : 1992-01-10
Application Number : 19962
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET, EXTENDED RELEASE...
Brand Name : TOPROL-XL
Dosage Strength : EQ 200MG TARTRATE
Packaging :
Approval Date : 1992-01-10
Application Number : 19962
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET, EXTENDED RELEASE...
Brand Name : TOPROL-XL
Dosage Strength : EQ 25MG TARTRATE
Packaging :
Approval Date : 2001-02-05
Application Number : 19962
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : POWDER;INTRAVENOUS
Brand Name : ORBACTIV
Dosage Strength : EQ 400MG BASE/VIAL
Packaging :
Approval Date : 2014-08-06
Application Number : 206334
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : POWDER;INTRAVENOUS
Brand Name : KIMYRSA
Dosage Strength : EQ 1.2GM BASE/VIAL
Packaging :
Approval Date : 2021-03-12
Application Number : 214155
Regulatory Info : RX
Registration Country : USA
