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    01 1ACAMPROSATE CALCIUM

    02 1ACETAMINOPHEN; IBUPROFEN

    03 1AMANTADINE HYDROCHLORIDE

    04 2AMPHETAMINE SULFATE

    05 2APIXABAN

    06 1ATOVAQUONE

    07 1AZELASTINE HYDROCHLORIDE

    08 3AZITHROMYCIN

    09 2BENZONATATE

    10 1BEXAROTENE

    11 1BROMPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PSEUDOEPHEDRINE HYDROCHLORIDE

    12 2CALCITRIOL

    13 1CARBAMAZEPINE

    14 5CETIRIZINE HYDROCHLORIDE

    15 1CEVIMELINE HYDROCHLORIDE

    16 4CIMETIDINE

    17 3CLOBAZAM

    18 1COLESEVELAM HYDROCHLORIDE

    19 3DEFERASIROX

    20 3DEXAMETHASONE

    21 2DEXMETHYLPHENIDATE HYDROCHLORIDE

    22 1DICLOFENAC POTASSIUM

    23 1DICYCLOMINE HYDROCHLORIDE

    24 1DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN

    25 3DOFETILIDE

    26 2DOXYCYCLINE HYCLATE

    27 1DOXYLAMINE SUCCINATE; PYRIDOXINE HYDROCHLORIDE

    28 3DROXIDOPA

    29 1ENALAPRIL MALEATE

    30 1ERGOCALCIFEROL

    31 2ESOMEPRAZOLE MAGNESIUM

    32 1ETHOSUXIMIDE

    33 2ETRAVIRINE

    34 1FAMOTIDINE

    35 2FEBUXOSTAT

    36 1FINGOLIMOD HYDROCHLORIDE

    37 5FLUVOXAMINE MALEATE

    38 3GRANISETRON HYDROCHLORIDE

    39 1HYDROXYZINE HYDROCHLORIDE

    40 2IBUPROFEN

    41 2IVABRADINE HYDROCHLORIDE

    42 1KETOROLAC TROMETHAMINE

    43 1LEVETIRACETAM

    44 1LIDOCAINE HYDROCHLORIDE

    45 4LOPERAMIDE HYDROCHLORIDE

    46 1LOPERAMIDE HYDROCHLORIDE; SIMETHICONE

    47 1LORATADINE

    48 1LORATADINE; PSEUDOEPHEDRINE SULFATE

    49 1MAGNESIUM SULFATE; POTASSIUM SULFATE; SODIUM SULFATE

    50 1METFORMIN HYDROCHLORIDE

    51 2METHIMAZOLE

    52 3METHYLPHENIDATE HYDROCHLORIDE

    53 1NAPROXEN SODIUM

    54 2NICARDIPINE HYDROCHLORIDE

    55 1NIMODIPINE

    56 1OXCARBAZEPINE

    57 3OXYBUTYNIN CHLORIDE

    58 3PARICALCITOL

    59 2POTASSIUM CITRATE

    60 2PROCHLORPERAZINE MALEATE

    61 2PROGESTERONE

    62 1RUFINAMIDE

    63 1SEVELAMER CARBONATE

    64 4TERAZOSIN HYDROCHLORIDE

    65 2TETRABENAZINE

    66 2THEOPHYLLINE

    67 1TRANEXAMIC ACID

    68 4VALPROIC ACID

    69 3ZONISAMIDE

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    01

    Brand Name : ACAMPROSATE CALCIUM

    U.S.A
    AAPS
    Not Confirmed
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    Brand Name : ACAMPROSATE CALCIUM

    U.S.A
    AAPS
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    RLD : No

    TE Code : AB

    ACAMPROSATE CALCIUM

    Bionpharma

    Dosage Form : TABLET, DELAYED RELEASE; ORAL

    Proprietary Name : ACAMPROSATE CALCIUM

    Dosage Strength : 333MG

    Approval Date : 2025-09-18

    Application Number : 219904

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    02

    Brand Name : ACETAMINOPHEN AND IB...

    U.S.A
    AAPS
    Not Confirmed
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    Brand Name : ACETAMINOPHEN AND IB...

    U.S.A
    AAPS
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    RLD : No

    TE Code :

    ACETAMINOPHEN; IBUPROFEN

    Bionpharma

    Dosage Form : TABLET; ORAL

    Proprietary Name : ACETAMINOPHEN AND IBUPRO...

    Dosage Strength : 250MG;125MG

    Approval Date : 2023-08-01

    Application Number : 216999

    RX/OTC/DISCN : OTC

    RLD : No

    TE Code :

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    03

    Brand Name : AMANTADINE HYDROCHLO...

    U.S.A
    AAPS
    Not Confirmed
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    Brand Name : AMANTADINE HYDROCHLO...

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    AAPS
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    RLD : No

    TE Code : AB

    AMANTADINE HYDROCHLORIDE

    Bionpharma

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : AMANTADINE HYDROCHLORIDE

    Dosage Strength : 100MG

    Approval Date : 2008-05-29

    Application Number : 78720

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    04

    Brand Name : AMPHETAMINE SULFATE

    U.S.A
    AAPS
    Not Confirmed
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    Brand Name : AMPHETAMINE SULFATE

    U.S.A
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    RLD : No

    TE Code : AA

    AMPHETAMINE SULFATE

    Bionpharma

    Dosage Form : TABLET; ORAL

    Proprietary Name : AMPHETAMINE SULFATE

    Dosage Strength : 5MG

    Approval Date : 2019-11-22

    Application Number : 212919

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AA

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    05

    Brand Name : AMPHETAMINE SULFATE

    U.S.A
    AAPS
    Not Confirmed
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    Brand Name : AMPHETAMINE SULFATE

    U.S.A
    AAPS
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    RLD : No

    TE Code : AA

    AMPHETAMINE SULFATE

    Bionpharma

    Dosage Form : TABLET; ORAL

    Proprietary Name : AMPHETAMINE SULFATE

    Dosage Strength : 10MG

    Approval Date : 2019-11-22

    Application Number : 212919

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AA

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    06

    Brand Name : APIXABAN

    U.S.A
    AAPS
    Not Confirmed
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    Brand Name : APIXABAN

    U.S.A
    AAPS
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    RLD : No

    TE Code :

    APIXABAN

    Bionpharma

    Dosage Form : TABLET; ORAL

    Proprietary Name : APIXABAN

    Dosage Strength : 2.5MG

    Approval Date : 2020-04-08

    Application Number : 210152

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    07

    Brand Name : APIXABAN

    U.S.A
    AAPS
    Not Confirmed
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    Brand Name : APIXABAN

    U.S.A
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    RLD : No

    TE Code :

    APIXABAN

    Bionpharma

    Dosage Form : TABLET; ORAL

    Proprietary Name : APIXABAN

    Dosage Strength : 5MG

    Approval Date : 2020-04-08

    Application Number : 210152

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    08

    Brand Name : ATOVAQUONE

    U.S.A
    AAPS
    Not Confirmed
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    Brand Name : ATOVAQUONE

    U.S.A
    AAPS
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    RLD : No

    TE Code : AB

    ATOVAQUONE

    Bionpharma

    Dosage Form : SUSPENSION; ORAL

    Proprietary Name : ATOVAQUONE

    Dosage Strength : 750MG/5ML

    Approval Date : 2021-03-30

    Application Number : 212918

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    09

    Brand Name : AZELASTINE HYDROCHLO...

    U.S.A
    AAPS
    Not Confirmed
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    Brand Name : AZELASTINE HYDROCHLO...

    U.S.A
    AAPS
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    RLD : No

    TE Code :

    AZELASTINE HYDROCHLORIDE

    Bionpharma

    Dosage Form : SPRAY, METERED; NASAL

    Proprietary Name : AZELASTINE HYDROCHLORIDE

    Dosage Strength : 0.137MG/SPRAY

    Approval Date : 2015-07-28

    Application Number : 90176

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    10

    Brand Name : AZITHROMYCIN

    U.S.A
    AAPS
    Not Confirmed
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    Brand Name : AZITHROMYCIN

    U.S.A
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    RLD : No

    TE Code : AB

    AZITHROMYCIN

    Bionpharma

    Dosage Form : TABLET; ORAL

    Proprietary Name : AZITHROMYCIN

    Dosage Strength : EQ 600MG BASE

    Approval Date : 2018-12-26

    Application Number : 209999

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    Contact Huhtamaki and get a quotation

    Huhtamaki is a supplier offers 3 products (APIs, Excipients or Intermediates).

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