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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

    Brand Name : AMANTADINE HYDROCHLO...

    U.S.A
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    Brand Name : AMANTADINE HYDROCHLO...

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    RLD : No

    TE Code : AB

    AMANTADINE HYDROCHLORIDE

    Puracap

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : AMANTADINE HYDROCHLORIDE

    Dosage Strength : 100MG

    Approval Date : 2022-12-20

    Application Number : 214580

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    02

    Brand Name : AMLODIPINE BESYLATE

    U.S.A
    CGT Asia
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    Brand Name : AMLODIPINE BESYLATE

    U.S.A
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    RLD : No

    TE Code : AB

    AMLODIPINE BESYLATE

    Puracap

    Dosage Form : TABLET; ORAL

    Proprietary Name : AMLODIPINE BESYLATE

    Dosage Strength : EQ 2.5MG BASE

    Approval Date : 2016-07-11

    Application Number : 207821

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    03

    Brand Name : AMLODIPINE BESYLATE

    U.S.A
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    RLD : No

    TE Code : AB

    AMLODIPINE BESYLATE

    Puracap

    Dosage Form : TABLET; ORAL

    Proprietary Name : AMLODIPINE BESYLATE

    Dosage Strength : EQ 5MG BASE

    Approval Date : 2016-07-11

    Application Number : 207821

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    04

    Brand Name : AMLODIPINE BESYLATE

    U.S.A
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    Brand Name : AMLODIPINE BESYLATE

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    RLD : No

    TE Code : AB

    AMLODIPINE BESYLATE

    Puracap

    Dosage Form : TABLET; ORAL

    Proprietary Name : AMLODIPINE BESYLATE

    Dosage Strength : EQ 10MG BASE

    Approval Date : 2016-07-11

    Application Number : 207821

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    05

    Brand Name : CALCITRIOL

    U.S.A
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    Brand Name : CALCITRIOL

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    RLD : No

    TE Code : AB

    CALCITRIOL

    Puracap

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : CALCITRIOL

    Dosage Strength : 0.25MCG

    Approval Date : 2026-02-27

    Application Number : 219796

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    06

    Brand Name : CALCITRIOL

    U.S.A
    CGT Asia
    Not Confirmed
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    RLD : No

    TE Code : AB

    CALCITRIOL

    Puracap

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : CALCITRIOL

    Dosage Strength : 0.5MCG

    Approval Date : 2026-02-27

    Application Number : 219796

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    07

    Brand Name : CLOPIDOGREL BISULFAT...

    U.S.A
    CGT Asia
    Not Confirmed
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    Brand Name : CLOPIDOGREL BISULFAT...

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    RLD : No

    TE Code : AB

    CLOPIDOGREL BISULFATE

    Puracap

    Dosage Form : TABLET; ORAL

    Proprietary Name : CLOPIDOGREL BISULFATE

    Dosage Strength : EQ 75MG BASE

    Approval Date : 2020-07-17

    Application Number : 213351

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    08

    Brand Name : CLOPIDOGREL BISULFAT...

    U.S.A
    CGT Asia
    Not Confirmed
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    Brand Name : CLOPIDOGREL BISULFAT...

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    RLD : No

    TE Code : AB

    CLOPIDOGREL BISULFATE

    Puracap

    Dosage Form : TABLET; ORAL

    Proprietary Name : CLOPIDOGREL BISULFATE

    Dosage Strength : EQ 300MG BASE

    Approval Date : 2020-07-17

    Application Number : 213351

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    09

    Brand Name : DARIFENACIN HYDROBRO...

    U.S.A
    CGT Asia
    Not Confirmed
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    Brand Name : DARIFENACIN HYDROBRO...

    U.S.A
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    RLD : No

    TE Code : AB

    DARIFENACIN HYDROBROMIDE

    Puracap

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : DARIFENACIN HYDROBROMIDE

    Dosage Strength : EQ 7.5MG BASE

    Approval Date : 2020-01-06

    Application Number : 211045

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    10

    Brand Name : DARIFENACIN HYDROBRO...

    U.S.A
    CGT Asia
    Not Confirmed
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    Brand Name : DARIFENACIN HYDROBRO...

    U.S.A
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    RLD : No

    TE Code : AB

    DARIFENACIN HYDROBROMIDE

    Puracap

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : DARIFENACIN HYDROBROMIDE

    Dosage Strength : EQ 15MG BASE

    Approval Date : 2020-01-06

    Application Number : 211045

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    • Product listings are provided for informational purposes only. We do not supply or sell any products. Any products that may be covered by patent(s) are supplied solely for uses permitted under Section 107A of the Indian Patents Act and not for commercial sale.