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01 1AMANTADINE HYDROCHLORIDE
02 3AMLODIPINE BESYLATE
03 2CLOPIDOGREL BISULFATE
04 2DARIFENACIN HYDROBROMIDE
05 1DUTASTERIDE
06 1IBUPROFEN
07 2ICOSAPENT ETHYL
08 2MEMANTINE HYDROCHLORIDE
09 1PHENTERMINE HYDROCHLORIDE
10 1TRAMADOL HYDROCHLORIDE
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01 5HUMANWELL PURACAP
02 11PURACAP LABS BLU
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01 5CAPSULE;ORAL
02 2TABLET, EXTENDED RELEASE;ORAL
03 9TABLET;ORAL
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01 10.5MG
02 1100MG
03 110MG
04 11GM
05 137.5MG
06 1500MG
07 150MG
08 15MG
09 1EQ 10MG BASE
10 1EQ 15MG BASE
11 1EQ 2.5MG BASE
12 1EQ 200MG FREE ACID AND POTASSIUM SALT
13 1EQ 300MG BASE
14 1EQ 5MG BASE
15 1EQ 7.5MG BASE
16 1EQ 75MG BASE
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01 16USA
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Regulatory Info : RX
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : AMANTADINE HYDROCHLORIDE
Dosage Strength : 100MG
Packaging :
Approval Date : 2022-12-20
Application Number : 214580
Regulatory Info : RX
Registration Country : USA

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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

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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

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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

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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

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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

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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

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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

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Regulatory Info : RX
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : DUTASTERIDE
Dosage Strength : 0.5MG
Packaging :
Approval Date : 2017-11-21
Application Number : 209909
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : OTC
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : IBUPROFEN
Dosage Strength : EQ 200MG FREE ACID AND...
Packaging :
Approval Date : 2016-06-21
Application Number : 206568
Regulatory Info : OTC
Registration Country : USA
