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01 4ALPELISIB

02 2ASCIMINIB (ASCIMINIB HYDROCHLORIDE)

03 1ATROPINE SULFATE

04 1BACLOFEN

05 1BASILIXIMAB

06 1BETAXOLOL (BETAXOLOL HYDROCHLORIDE)

07 1BRIMONIDINE TARTRATE

08 3BRINZOLAMIDE

09 1BROLUCIZUMAB

10 2CALCIUM CHLORIDE

11 1CANAKINUMAB

12 2CAPMATINIB (CAPMATINIB HYDROCHLORIDE)

13 1CARBACHOL

14 4CARBAMAZEPINE

15 1CERITINIB

16 3CIPROFLOXACIN (CIPROFLOXACIN HYDROCHLORIDE)

17 1CYCLOPENTOLATE HYDROCHLORIDE

18 6CYCLOSPORINE

19 3DABRAFENIB (DABRAFENIB MESYLATE)

20 6DEFERASIROX

21 1DEFEROXAMINE MESYLATE

22 7DEXAMETHASONE

23 3DEXTRAN 70

24 1DEXTROSE

25 1DICLOFENAC POTASSIUM

26 3DICLOFENAC SODIUM

27 1DIFLUPREDNATE

28 2ELTROMBOPAG (ELTROMBOPAG OLAMINE)

29 2ERENUMAB

30 6EVEROLIMUS

31 2FINGOLIMOD (FINGOLIMOD HYDROCHLORIDE)

32 1FLUORESCEIN (FLUORESCEIN SODIUM)

33 1FLUOROMETHOLONE ACETATE

34 1GALLIUM (68Ga) GOZETOTIDE

35 1GLUTATHIONE DISULFIDE

36 1GLYCERINE

37 3GLYCOPYRRONIUM (GLYCOPYRRONIUM BROMIDE)

38 5HYDROCHLOROTHIAZIDE

39 6HYPROMELLOSE

40 2IMATINIB (IMATINIB MESYLATE)

41 1INCLISIRAN (INCLISIRAN SODIUM)

42 4INDACATEROL (INDACATEROL ACETATE)

43 1INDACATEROL (INDACATEROL MALEATE)

44 1LANOLIN

45 1LAPATINIB (LAPATINIB DITOSYLATE)

46 1LETROZOLE

47 1LIFITEGRAST

48 1LODOXAMIDE (LODOXAMIDE TROMETHAMINE)

49 1LUTETIUM (177LU) OXODOTREOTIDE

50 1LUTETIUM (177LU) VIPIVOTIDE TETRAXETAN

51 2MAGNESIUM CHLORIDE

52 1MIDOSTAURIN

53 1MINERAL OIL

54 4MOMETASONE FUROATE

55 1MOXIFLOXACIN (MOXIFLOXACIN HYDROCHLORIDE)

56 2MYCOPHENOLIC ACID (MYCOPHENOLATE SODIUM)

57 1NAPHAZOLINE HYDROCHLORIDE

58 2NEOMYCIN (NEOMYCIN SULFATE)

59 2NEPAFENAC

60 2NILOTINIB (NILOTINIB HYDROCHLORIDE MONOHYDRATE)

61 4OCTREOTIDE (OCTREOTIDE ACETATE)

62 1OFATUMUMAB

63 3OLOPATADINE (OLOPATADINE HYDROCHLORIDE)

64 3OMALIZUMAB

65 1ONASEMNOGENE ABEPARVOVEC

66 3OXCARBAZEPINE

67 1OXODOTREOTIDE

68 1PAZOPANIB (PAZOPANIB HYDROCHLORIDE)

69 1PHENIRAMINE MALEATE

70 1PHENYLEPHRINE HYDROCHLORIDE

71 1PILOCARPINE HYDROCHLORIDE

72 1POLYETHYLENE GLYCOL 400

73 2POLYMYXIN B SULFATE

74 2POTASSIUM CHLORIDE

75 1PROPARACAINE HYDROCHLORIDE

76 1PROPYLENE GLYCOL

77 2RANIBIZUMAB

78 1RIBOCICLIB (RIBOCICLIB SUCCINATE)

79 4RUXOLITINIB (RUXOLITINIB PHOSPHATE)

80 3SACUBITRIL (SACUBITRIL VALSARTAN SODIUM HYDRATE COMPLEX)

81 2SECUKINUMAB

82 2SIPONIMOD

83 1SODIUM ACETATE TRIHYDRATE

84 1SODIUM BICARBONATE

85 2SODIUM CHLORIDE

86 1SODIUM CITRATE DIHYDRATE

87 1SODIUM PHOSPHATE DIBASIC

88 1TERBINAFINE (TERBINAFINE HYDROCHLORIDE)

89 2TERBINAFINE HYDROCHLORIDE

90 2TIMOLOL (TIMOLOL MALEATE)

91 1TISAGENLECLEUCEL

92 4TOBRAMYCIN

93 3TRAMETINIB

94 3TRAVOPROST

95 1TRIAMCINOLONE ACETONIDE

96 2TROPICAMIDE

97 9VALSARTAN

98 3VALSARTAN (SACUBITRIL VALSARTAN SODIUM HYDRATE COMPLEX)

99 1VORETIGENE NEPARVOVEC

100 1WHITE PETROLATUM

101 1ZOLEDRONIC ACID (ZOLEDRONIC ACID MONOHYDRATE)

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PharmaCompass

01

Brand Name : LIORESAL INTRATHECAL...

euroPLX 86 Munich
Not Confirmed
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Brand Name : LIORESAL INTRATHECAL...

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euroPLX 86 Munich
Not Confirmed

Novartis Pharmaceuticals Corporation

Dosage Form : SOLUTION

Dosage Strength : 0.05MG/ML

Packaging : 1ML

Brand Name : LIORESAL INTRATHECAL 0.05MG/M...

Approval Date :

Application Number : 2131048

Regulatory Info : Prescription

Registration Country : Canada

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02

Brand Name : BETOPTIC S

euroPLX 86 Munich
Not Confirmed
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Brand Name : BETOPTIC S

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euroPLX 86 Munich
Not Confirmed

Novartis Pharmaceuticals Corporation

Dosage Form : SUSPENSION

Dosage Strength : 0.25%/W/V

Packaging : 5ML/10ML

Brand Name : BETOPTIC S

Approval Date :

Application Number : 1908448

Regulatory Info : Prescription

Registration Country : Canada

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03

Brand Name : ALCON ATROPINE

euroPLX 86 Munich
Not Confirmed
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Brand Name : ALCON ATROPINE

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euroPLX 86 Munich
Not Confirmed

Alcon Inc

Dosage Form : SOLUTION

Dosage Strength : 1%/W/V

Packaging : 5 ML

Brand Name : ALCON ATROPINE

Approval Date :

Application Number : 35017

Regulatory Info : Prescription

Registration Country : Canada

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04

Brand Name : SIMULECT

euroPLX 86 Munich
Not Confirmed
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Brand Name : SIMULECT

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euroPLX 86 Munich
Not Confirmed

Novartis Pharmaceuticals Corporation

Dosage Form : POWDER FOR SOLUTION

Dosage Strength : 20MG/VIAL

Packaging : 5ML

Brand Name : SIMULECT

Approval Date :

Application Number : 2242815

Regulatory Info : Prescription

Registration Country : Canada

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05

Brand Name : PIQRAY

euroPLX 86 Munich
Not Confirmed
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Brand Name : PIQRAY

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euroPLX 86 Munich
Not Confirmed

Novartis Pharmaceuticals Corporation

Dosage Form : TABLET

Dosage Strength : 150MG

Packaging :

Brand Name : PIQRAY

Approval Date :

Application Number : 2497069

Regulatory Info : Prescription

Registration Country : Canada

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06

Brand Name : PIQRAY

euroPLX 86 Munich
Not Confirmed
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Brand Name : PIQRAY

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euroPLX 86 Munich
Not Confirmed

Novartis Pharmaceuticals Corporation

Dosage Form : TABLET

Dosage Strength : 200MG

Packaging :

Brand Name : PIQRAY

Approval Date :

Application Number : 2497077

Regulatory Info : Prescription

Registration Country : Canada

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07

Brand Name : PIQRAY

euroPLX 86 Munich
Not Confirmed
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Brand Name : PIQRAY

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euroPLX 86 Munich
Not Confirmed

Novartis Pharmaceuticals Corporation

Dosage Form : KIT

Dosage Strength : 50MG

Packaging :

Brand Name : PIQRAY

Approval Date :

Application Number : 2497085

Regulatory Info : Prescription

Registration Country : Canada

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08

Brand Name : PIQRAY

euroPLX 86 Munich
Not Confirmed
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Brand Name : PIQRAY

arrow
euroPLX 86 Munich
Not Confirmed

Novartis Pharmaceuticals Corporation

Dosage Form : KIT

Dosage Strength : 200MG

Packaging :

Brand Name : PIQRAY

Approval Date :

Application Number : 2497085

Regulatory Info : Prescription

Registration Country : Canada

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09

Brand Name : SCEMBLIX

euroPLX 86 Munich
Not Confirmed
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Brand Name : SCEMBLIX

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euroPLX 86 Munich
Not Confirmed

Novartis Pharmaceuticals Corporation

Dosage Form : TABLET

Dosage Strength : 20MG

Packaging :

Brand Name : SCEMBLIX

Approval Date :

Application Number : 2528320

Regulatory Info : Prescription

Registration Country : Canada

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10

Brand Name : SCEMBLIX

euroPLX 86 Munich
Not Confirmed
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Brand Name : SCEMBLIX

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euroPLX 86 Munich
Not Confirmed

Novartis Pharmaceuticals Corporation

Dosage Form : TABLET

Dosage Strength : 40MG

Packaging :

Brand Name : SCEMBLIX

Approval Date :

Application Number : 2528339

Regulatory Info : Prescription

Registration Country : Canada

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Contact Novartis Pharmaceuticals Corporation and get a quotation

Novartis Pharmaceuticals Corporation is a supplier offers 41 products (APIs, Excipients or Intermediates).

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