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01 3EPTIFIBATIDE
02 1Klopidogrelv?tesulfat
03 1OLOPATADINE HYDROCHLORIDE
04 1ZOLEDRONIC ACID
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01 5USV
02 1Usv Europa Ltd
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01 1Film Coated Tablet
02 3INJECTABLE;INJECTION
03 1INJECTABLE;INTRAVENOUS
04 1SOLUTION/DROPS;OPHTHALMIC
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01 22MG/ML
02 175MG/100ML
03 175mg
04 1EQ 0.1% BASE
05 1EQ 4MG BASE/5ML
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01 1Sweden
02 5USA
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Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : EPTIFIBATIDE
Dosage Strength : 2MG/ML
Packaging :
Approval Date : 2019-03-14
Application Number : 204361
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : EPTIFIBATIDE
Dosage Strength : 75MG/100ML
Packaging :
Approval Date : 2019-03-14
Application Number : 204361
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : EPTIFIBATIDE
Dosage Strength : 2MG/ML
Packaging :
Approval Date : 2019-03-11
Application Number : 204362
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Film Coated Tablet
Brand Name : Clopidogrel Usv Europe
Dosage Strength : 75mg
Packaging :
Approval Date : 11-10-2012
Application Number : 2.01E+13
Regulatory Info : Deregistered
Registration Country : Sweden

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Regulatory Info : OTC
Registration Country : USA
Dosage Form : SOLUTION/DROPS;OPHTHALMI...
Brand Name : OLOPATADINE HYDROCHLORIDE
Dosage Strength : EQ 0.1% BASE
Packaging :
Approval Date : 2015-12-07
Application Number : 203152
Regulatory Info : OTC
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INTRAVENOUS
Brand Name : ZOLEDRONIC ACID
Dosage Strength : EQ 4MG BASE/5ML
Packaging :
Approval Date : 2014-09-04
Application Number : 202923
Regulatory Info : RX
Registration Country : USA

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