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01 1AMANTADINE HYDROCHLORIDE
02 3AMLODIPINE BESYLATE
03 2CALCITRIOL
04 2CLOPIDOGREL BISULFATE
05 2DARIFENACIN HYDROBROMIDE
06 1DUTASTERIDE
07 1IBUPROFEN
08 2ICOSAPENT ETHYL
09 2MEMANTINE HYDROCHLORIDE
10 1PHENTERMINE HYDROCHLORIDE
11 1TRAMADOL HYDROCHLORIDE
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01 7HUMANWELL PURACAP
02 11PURACAP LABS BLU
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01 7CAPSULE;ORAL
02 2TABLET, EXTENDED RELEASE;ORAL
03 9TABLET;ORAL
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01 10.25MCG
02 10.5MCG
03 10.5MG
04 1100MG
05 110MG
06 11GM
07 137.5MG
08 1500MG
09 150MG
10 15MG
11 1EQ 10MG BASE
12 1EQ 15MG BASE
13 1EQ 2.5MG BASE
14 1EQ 200MG FREE ACID AND POTASSIUM SALT
15 1EQ 300MG BASE
16 1EQ 5MG BASE
17 1EQ 7.5MG BASE
18 1EQ 75MG BASE
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01 18USA
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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 : CAPSULE;ORAL
Brand Name : CALCITRIOL
Dosage Strength : 0.25MCG
Packaging :
Approval Date : 2026-02-27
Application Number : 219796
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : CALCITRIOL
Dosage Strength : 0.5MCG
Packaging :
Approval Date : 2026-02-27
Application Number : 219796
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
