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    Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.

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    Minakem delivers API, HPAPI, steroids & CDMO services for generics with FDA/GMP certification, regulatory know-how & proven success.

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    IKF/Pharmasynthese have been with fine chemicals market and APIs performance for more than 40 years.

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    Cosma S.p.A., part of CFM Group with AMSA & Clarochem, provides global pharma & veterinary health with 300+ tons of FDA-approved APIs.

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    TWi Pharmaceuticals

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    01 3ATENOLOL

    02 2ATENOLOL; CHLORTHALIDONE

    03 3BUPROPION HYDROCHLORIDE

    04 2CHOLINE FENOFIBRATE

    05 2CYCLOBENZAPRINE HYDROCHLORIDE

    06 1CYCLOSPORINE

    07 2DEXLANSOPRAZOLE

    08 1DICLOFENAC SODIUM

    09 2DICYCLOMINE HYDROCHLORIDE

    10 8DILTIAZEM HYDROCHLORIDE

    11 2DIMETHYL FUMARATE

    12 1DONEPEZIL HYDROCHLORIDE

    13 1FLUOXETINE HYDROCHLORIDE

    14 4FLUPHENAZINE HYDROCHLORIDE

    15 4GUANFACINE HYDROCHLORIDE

    16 6LISINOPRIL

    17 1MEGESTROL ACETATE

    18 2METFORMIN HYDROCHLORIDE

    19 2MYCOPHENOLATE SODIUM

    20 3NAPROXEN SODIUM

    21 3NIFEDIPINE

    22 3OXCARBAZEPINE

    23 4POTASSIUM CHLORIDE

    24 3PROPAFENONE HYDROCHLORIDE

    25 2TERBUTALINE SULFATE

    26 2TESTOSTERONE

    27 2TOPIRAMATE

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    01

    Brand Name : TENORMIN

    Taiwan
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    Brand Name : TENORMIN

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    RLD : Yes

    TE Code : AB

    ATENOLOL

    TWi Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : TENORMIN

    Dosage Strength : 50MG

    Approval Date : 1982-01-01

    Application Number : 18240

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    02

    Brand Name : TENORMIN

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    RLD : Yes

    TE Code : AB

    ATENOLOL

    TWi Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : TENORMIN

    Dosage Strength : 100MG

    Approval Date : 1982-01-01

    Application Number : 18240

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    03

    Brand Name : TENORMIN

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    RLD : Yes

    TE Code : AB

    ATENOLOL

    TWi Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : TENORMIN

    Dosage Strength : 25MG

    Approval Date : 1990-04-09

    Application Number : 18240

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    04

    Brand Name : TENORETIC 100

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    RLD : Yes

    TE Code : AB

    ATENOLOL; CHLORTHALIDONE

    TWi Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : TENORETIC 100

    Dosage Strength : 100MG;25MG

    Approval Date : 1984-06-08

    Application Number : 18760

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    05

    Brand Name : TENORETIC 50

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    RLD : Yes

    TE Code : AB

    ATENOLOL; CHLORTHALIDONE

    TWi Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : TENORETIC 50

    Dosage Strength : 50MG;25MG

    Approval Date : 1984-06-08

    Application Number : 18760

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    06

    Brand Name : FORFIVO XL

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    RLD : Yes

    TE Code :

    BUPROPION HYDROCHLORIDE

    TWi Pharmaceuticals

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : FORFIVO XL

    Dosage Strength : 450MG

    Approval Date : 2011-11-10

    Application Number : 22497

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    07

    Brand Name : BUPROPION HYDROCHLOR...

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    RLD : No

    TE Code :

    BUPROPION HYDROCHLORIDE

    TWi Pharmaceuticals

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : BUPROPION HYDROCHLORIDE

    Dosage Strength : 150MG

    Approval Date : 2017-11-03

    Application Number : 210081

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    Brand Name : BUPROPION HYDROCHLOR...

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    RLD : No

    TE Code :

    BUPROPION HYDROCHLORIDE

    TWi Pharmaceuticals

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : BUPROPION HYDROCHLORIDE

    Dosage Strength : 300MG

    Approval Date : 2017-11-03

    Application Number : 210081

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    09

    Brand Name : FENOFIBRIC ACID

    Taiwan
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    Brand Name : FENOFIBRIC ACID

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    RLD : No

    TE Code :

    CHOLINE FENOFIBRATE

    TWi Pharmaceuticals

    Dosage Form : CAPSULE, DELAYED RELEASE; ORAL

    Proprietary Name : FENOFIBRIC ACID

    Dosage Strength : EQ 45MG FENOFIBRIC ACID

    Approval Date : 2019-07-05

    Application Number : 210469

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    Brand Name : FENOFIBRIC ACID

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    RLD : No

    TE Code :

    CHOLINE FENOFIBRATE

    TWi Pharmaceuticals

    Dosage Form : CAPSULE, DELAYED RELEASE; ORAL

    Proprietary Name : FENOFIBRIC ACID

    Dosage Strength : EQ 135MG FENOFIBRIC ACID

    Approval Date : 2019-07-05

    Application Number : 210469

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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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.