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    Bloomage is a one-stop source for CEP Sodium Hyaluronate and Hyaluronic Acid// FDA-inspected & GMP-certified.

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    ACTIVE PHARMA INGREDIENTS

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    01 1BENZTROPINE MESYLATE

    02 1CARGLUMIC ACID

    03 1CARMUSTINE

    04 3DIAZEPAM

    05 1FAMOTIDINE

    06 1FOMEPIZOLE

    07 1FOSAPREPITANT DIMEGLUMINE

    08 1HYDRALAZINE HYDROCHLORIDE

    09 1INDOMETHACIN SODIUM

    10 2MARAVIROC

    11 1METHOCARBAMOL

    12 1MIGLUSTAT

    13 3NICARDIPINE HYDROCHLORIDE

    14 1PENICILLAMINE

    15 1RIBAVIRIN

    16 3ROPIVACAINE HYDROCHLORIDE

    17 1SEVELAMER CARBONATE

    18 1SEVELAMER HYDROCHLORIDE

    19 2SODIUM BENZOATE; SODIUM PHENYLACETATE

    20 1TRIENTINE HYDROCHLORIDE

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    01

    Brand Name : BENZTROPINE MESYLATE

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    Brand Name : BENZTROPINE MESYLATE

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    Regulatory Info : RX

    Registration Country : USA

    BENZTROPINE MESYLATE

    Navinta

    Dosage Form : INJECTABLE;INJECTION

    Brand Name : BENZTROPINE MESYLATE

    Dosage Strength : 1MG/ML

    Packaging :

    Approval Date : 2013-02-05

    Application Number : 91525

    Regulatory Info : RX

    Registration Country : USA

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    02

    Brand Name : CARGLUMIC ACID

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    Brand Name : CARGLUMIC ACID

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    Regulatory Info : RX

    Registration Country : USA

    CARGLUMIC ACID

    Navinta

    Dosage Form : TABLET, FOR SUSPENSION;O...

    Brand Name : CARGLUMIC ACID

    Dosage Strength : 200MG

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    Approval Date : 2022-06-22

    Application Number : 213395

    Regulatory Info : RX

    Registration Country : USA

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    03

    Brand Name : CARMUSTINE

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    Regulatory Info : RX

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    CARMUSTINE

    Navinta

    Dosage Form : INJECTABLE;INJECTION

    Brand Name : CARMUSTINE

    Dosage Strength : 100MG/VIAL

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    Approval Date : 2018-09-11

    Application Number : 210179

    Regulatory Info : RX

    Registration Country : USA

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    04

    Brand Name : DIAZEPAM

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    Regulatory Info :

    Registration Country : USA

    DIAZEPAM

    Navinta

    Dosage Form : GEL;RECTAL

    Brand Name : DIAZEPAM

    Dosage Strength : 2.5MG/0.5ML (5MG/ML)

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    Approval Date :

    Application Number : 217468

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    Registration Country : USA

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    05

    Brand Name : DIAZEPAM

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    Registration Country : USA

    DIAZEPAM

    Navinta

    Dosage Form : GEL;RECTAL

    Brand Name : DIAZEPAM

    Dosage Strength : 10MG/2ML (5MG/ML)

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    Approval Date :

    Application Number : 217468

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    Registration Country : USA

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    06

    Brand Name : DIAZEPAM

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    Regulatory Info :

    Registration Country : USA

    DIAZEPAM

    Navinta

    Dosage Form : GEL;RECTAL

    Brand Name : DIAZEPAM

    Dosage Strength : 20MG/4ML (5MG/ML)

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    Approval Date :

    Application Number : 217468

    Regulatory Info :

    Registration Country : USA

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    07

    Brand Name : FAMOTIDINE

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    Brand Name : FAMOTIDINE

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    Regulatory Info : RX

    Registration Country : USA

    FAMOTIDINE

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    Dosage Form : FOR SUSPENSION;ORAL

    Brand Name : FAMOTIDINE

    Dosage Strength : 40MG/5ML

    Packaging :

    Approval Date : 2010-05-27

    Application Number : 91020

    Regulatory Info : RX

    Registration Country : USA

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    08

    Brand Name : FOMEPIZOLE

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    Brand Name : FOMEPIZOLE

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    Regulatory Info : RX

    Registration Country : USA

    FOMEPIZOLE

    Navinta

    Dosage Form : INJECTABLE;INJECTION

    Brand Name : FOMEPIZOLE

    Dosage Strength : 1.5GM/1.5ML (1GM/ML)

    Packaging :

    Approval Date : 2008-03-06

    Application Number : 78537

    Regulatory Info : RX

    Registration Country : USA

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    09

    Brand Name : FOSAPREPITANT DIMEGL...

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    Regulatory Info : DISCN

    Registration Country : USA

    FOSAPREPITANT DIMEGLUMINE

    Navinta

    Dosage Form : POWDER;INTRAVENOUS

    Brand Name : FOSAPREPITANT DIMEGLUMINE

    Dosage Strength : EQ 150MG BASE/VIAL

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    Approval Date : 2020-08-20

    Application Number : 212957

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    Brand Name : HYDRALAZINE HYDROCHL...

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    Brand Name : HYDRALAZINE HYDROCHL...

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    Regulatory Info : RX

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    HYDRALAZINE HYDROCHLORIDE

    Navinta

    Dosage Form : INJECTABLE;INJECTION

    Brand Name : HYDRALAZINE HYDROCHLORIDE

    Dosage Strength : 20MG/ML

    Packaging :

    Approval Date : 2013-03-28

    Application Number : 202938

    Regulatory Info : RX

    Registration Country : USA

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    Contact Navinta and get a quotation

    Navinta is a supplier offers 9 products (APIs, Excipients or Intermediates).

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