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    01 5*ANTIHEMOPHILIC FACTOR VIII (RECOMBINANT, BDD), FC-VWF-XTEN FUSION PROTEIN

    02 1ACETAMINOPHEN

    03 2AGALSIDASE BETA

    04 2ALEMTUZUMAB

    05 1ALFUZOSIN HYDROCHLORIDE

    06 1ALGLUCOSIDASE ALFA

    07 3ALIROCUMAB

    08 1ANTI-THYMOCYTE GLOBULIN (RABBIT)

    09 7ANTIHEMOPHILIC FACTOR (RECOMBINANT BDD), FC FUSION PROTEIN

    10 1AVALGLUCOSIDASE ALFA

    11 1BELUMOSUDIL (BELUMOSUDIL MESYLATE)

    12 3BISACODYL

    13 1CALCITONIN (SALMON SYNTHETIC)

    14 1CALCIUM POLYSTYRENE SULFONATE

    15 1CLOFARABINE

    16 1CLOPIDOGREL (CLOPIDOGREL BISULFATE)

    17 1CODEINE PHOSPHATE

    18 2DANAZOL

    19 1DIMETHICONE

    20 4DIPHTHERIA TOXOID

    21 1DIPHTHERIA TOXOID ADSORBED

    22 1DOXYLAMINE SUCCINATE

    23 1DRONEDARONE (DRONEDARONE HYDROCHLORIDE)

    24 4DUPILUMAB

    25 1ELIGLUSTAT (ELIGLUSTAT TARTRATE)

    26 8ENOXAPARIN SODIUM

    27 4FEXOFENADINE HYDROCHLORIDE

    28 4FILAMENTOUS HAEMAGGLUTININ

    29 1FIMBRIAE

    30 3FIMBRIAE TYPES 2 AND 3 (FIM)

    31 1FLUDARABINE PHOSPHATE

    32 2FUROSEMIDE

    33 6HAEMAGGLUTININ-STRAIN A (H1N1)

    34 6HAEMAGGLUTININ-STRAIN A (H3N2)

    35 3HAEMAGGLUTININ-STRAIN B

    36 3HAEMAGGLUTININ-STRAIN B (VICTORIA)

    37 3HAEMAGGLUTININ-STRAIN B (YAMAGATA)

    38 2HAEMOPHILUS INFLUENZAE TYPE B-PRP

    39 1HEPATITIS A VIRUS, INACTIVATED

    40 2HYDROCHLOROTHIAZIDE

    41 1HYDROXYCHLOROQUINE SULFATE

    42 2HYOSCINE BUTYLBROMIDE

    43 1IMIGLUCERASE

    44 1INACTIVATED RABIES VIRUS (PM/WI38 1503-3M)

    45 3INSULIN ASPART

    46 6INSULIN GLARGINE

    47 3INSULIN GLULISINE (RECOMBINANT DNA ORIGIN)

    48 3INSULIN LISPRO

    49 4IRBESARTAN

    50 1IRON (SODIUM FERRIC GLUCONATE COMPLEX IN SUCROSE INJECTION)

    51 2ISATUXIMAB

    52 1LARONIDASE

    53 2LEFLUNOMIDE

    54 1LIDOCAINE HYDROCHLORIDE

    55 1LIXISENATIDE

    56 1MENINGOCOCCAL GROUP A POLYSACCHARIDE-TETANUS TOXOID CONJUGATE

    57 1MENINGOCOCCAL GROUP C POLYSACCHARIDE-TETANUS TOXOID CONJUGATE

    58 1MENINGOCOCCAL GROUP W POLYSACCHARIDE-TETANUS TOXOID CONJUGATE

    59 1MENINGOCOCCAL GROUP Y POLYSACCHARIDE-TETANUS TOXOID CONJUGATE

    60 1MENINGOCOCCAL POLYSACCHARIDE-DIPHTHERIA TOXOID CONJUGATE, GROUP A

    61 1MENINGOCOCCAL POLYSACCHARIDE-DIPHTHERIA TOXOID CONJUGATE, GROUP C

    62 1MENINGOCOCCAL POLYSACCHARIDE-DIPHTHERIA TOXOID CONJUGATE, GROUP W 135

    63 1MENINGOCOCCAL POLYSACCHARIDE-DIPHTHERIA TOXOID CONJUGATE, GROUP Y

    64 2MENTHOL

    65 2METFORMIN HYDROCHLORIDE

    66 1METOLAZONE

    67 1METRONIDAZOLE

    68 2NIRSEVIMAB

    69 1NITROGLYCERIN

    70 1NYSTATIN

    71 1OLIPUDASE ALFA

    72 4PERTACTIN

    73 4PERTUSSIS TOXOID

    74 4POLIOVIRUS TYPE 1 MAHONEY (INACTIVATED)

    75 4POLIOVIRUS TYPE 2 MEF1 (INACTIVATED)

    76 4POLIOVIRUS TYPE 3 SAUKETT (INACTIVATED)

    77 2PRAMOXINE HYDROCHLORIDE

    78 1PRIMAQUINE PHOSPHATE

    79 1PSEUDOEPHEDRINE HYDROCHLORIDE

    80 1PURIFIED PROTEIN DERIVATIVE OF TUBERCULIN

    81 1PYRITHIONE ZINC

    82 1RASBURICASE

    83 4RECOMBINANT HUMAN COAGULATION FACTOR IX, FC FUSION PROTEIN

    84 1RILUZOLE

    85 1SALMONELLA TYPHI TY2 VI CAPSULAR POLYSACCHARIDE

    86 3SARILUMAB

    87 1SEVELAMER CARBONATE

    88 1SEVELAMER HYDROCHLORIDE

    89 1SODIUM POLYSTYRENE SULFONATE

    90 1TEPLIZUMAB

    91 2TETANUS PROTEIN

    92 5TETANUS TOXOID

    93 1TETANUS TOXOID ADSORBED

    94 1THYROTROPIN ALFA

    95 2TRIAMCINOLONE ACETONIDE

    96 1TROLAMINE SALICYLATE

    97 2VANDETANIB

    98 1WHITE PETROLATUM

    99 1YELLOW FEVER VACCINE

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    Brand Name : MERSYNDOL WITH CODEI...

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    Regulatory Info : NARCOTICS (CDSA I)

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    Dosage Form : TABLET

    Dosage Strength : 325MG

    Packaging : 24/100

    Brand Name : MERSYNDOL WITH CODEINE

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    Application Number : 2047667

    Regulatory Info : NARCOTICS (CDSA I)

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    Brand Name : FABRAZYME

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    Regulatory Info : SCHEDULE D

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    AGALSIDASE BETA

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    Dosage Form : POWDER FOR SOLUTION

    Dosage Strength : 5MG/VIAL

    Packaging : 1.1ML

    Brand Name : FABRAZYME

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    Application Number : 2248965

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    Brand Name : FABRAZYME

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    Regulatory Info : SCHEDULE D

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    Dosage Form : POWDER FOR SOLUTION

    Dosage Strength : 35MG/VIAL

    Packaging : 7.2ML

    Brand Name : FABRAZYME

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    Application Number : 2248966

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    Brand Name : MABCAMPATH

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    Regulatory Info : SCHEDULE D

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    ALEMTUZUMAB

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    Dosage Form : SOLUTION

    Dosage Strength : 30MG/ML

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    Brand Name : MABCAMPATH

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    Application Number : 2290960

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    Brand Name : LEMTRADA

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    Regulatory Info : SCHEDULE D

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    ALEMTUZUMAB

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    Dosage Form : SOLUTION

    Dosage Strength : 12MG/1.2ML

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    Brand Name : LEMTRADA

    Approval Date :

    Application Number : 2418320

    Regulatory Info : SCHEDULE D

    Registration Country : Canada

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    Brand Name : ALTUVIIIO

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    Regulatory Info : SCHEDULE D

    Registration Country : Canada

    *ANTIHEMOPHILIC FACTOR VIII (RECOMBINANT, BDD), FC...

    Sanofi

    Dosage Form : POWDER FOR SOLUTION

    Dosage Strength : 3000UNIT/VIAL

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    Brand Name : ALTUVIIIO

    Approval Date :

    Application Number : 2447967

    Regulatory Info : SCHEDULE D

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    Brand Name : ALTUVIIIO

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    Regulatory Info : SCHEDULE D

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    *ANTIHEMOPHILIC FACTOR VIII (RECOMBINANT, BDD), FC...

    Sanofi

    Dosage Form : POWDER FOR SOLUTION

    Dosage Strength : 500UNIT/VIAL

    Packaging :

    Brand Name : ALTUVIIIO

    Approval Date :

    Application Number : 2448122

    Regulatory Info : SCHEDULE D

    Registration Country : Canada

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    Brand Name : ALTUVIIIO

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    Regulatory Info : PRESCRIPTION

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    *ANTIHEMOPHILIC FACTOR VIII (RECOMBINANT, BDD), FC...

    Sanofi

    Dosage Form : POWDER FOR SOLUTION

    Dosage Strength : 1000UNIT/VIAL

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    Brand Name : ALTUVIIIO

    Approval Date :

    Application Number : 2448130

    Regulatory Info : PRESCRIPTION

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    Brand Name : ALTUVIIIO

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    *ANTIHEMOPHILIC FACTOR VIII (RECOMBINANT, BDD), FC...

    Sanofi

    Dosage Form : POWDER FOR SOLUTION

    Dosage Strength : 2000UNIT/VIAL

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    Brand Name : ALTUVIIIO

    Approval Date :

    Application Number : 2448149

    Regulatory Info : PRESCRIPTION

    Registration Country : Canada

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    Brand Name : ALTUVIIIO

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    *ANTIHEMOPHILIC FACTOR VIII (RECOMBINANT, BDD), FC...

    Sanofi

    Dosage Form : POWDER FOR SOLUTION

    Dosage Strength : 4000UNIT/VIAL

    Packaging :

    Brand Name : ALTUVIIIO

    Approval Date :

    Application Number : 2448157

    Regulatory Info : SCHEDULE D

    Registration Country : Canada

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    Sanofi is a supplier offers 203 products (APIs, Excipients or Intermediates).

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