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01 1ABBVIE CORPORATION

02 2NOVO NORDISK CANADA INC

03 2SANDOZ CANADA INCORPORATED

04 1SEARCHLIGHT PHARMA INC

05 1SUMITOMO PHARMA SWITZERLAND GMBH

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PharmaCompass

01

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euroPLX 86 Munich
Not Confirmed

NORETHINDRONE ACETATE

Brand Name : LOLO

Dosage Form : TABLET

Dosage Strength : 1MG

Packaging :

Approval Date :

Application Number : 2417456

Regulatory Info : Prescription

Registration Country : Canada

Abbvie Company Banner

02

euroPLX 86 Munich
Not Confirmed
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euroPLX 86 Munich
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NORETHINDRONE ACETATE

Brand Name : ACTIVELLE

Dosage Form : TABLET

Dosage Strength : 0.5MG

Packaging : 28

Approval Date :

Application Number : 2249405

Regulatory Info : Prescription

Registration Country : Canada

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euroPLX 86 Munich
Not Confirmed
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euroPLX 86 Munich
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NORETHINDRONE ACETATE

Brand Name : ACTIVELLE LD

Dosage Form : TABLET

Dosage Strength : 0.1MG

Packaging : 28

Approval Date :

Application Number : 2309009

Regulatory Info : Prescription

Registration Country : Canada

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04

euroPLX 86 Munich
Not Confirmed
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euroPLX 86 Munich
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NORETHINDRONE ACETATE

Brand Name : ESTALIS 250/50 MCG

Dosage Form : PATCH

Dosage Strength : 250MCG/24HOUR

Packaging : 8

Approval Date :

Application Number : 2241837

Regulatory Info : Prescription

Registration Country : Canada

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05

euroPLX 86 Munich
Not Confirmed
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euroPLX 86 Munich
Not Confirmed

NORETHINDRONE ACETATE

Brand Name : ESTALIS 140/50 MCG

Dosage Form : PATCH

Dosage Strength : 140MCG/24HOUR

Packaging : 8

Approval Date :

Application Number : 2241835

Regulatory Info : Prescription

Registration Country : Canada

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06

euroPLX 86 Munich
Not Confirmed
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euroPLX 86 Munich
Not Confirmed

NORETHINDRONE ACETATE

Brand Name : NORLUTATE

Dosage Form : TABLET

Dosage Strength : 5MG

Packaging : 30

Approval Date :

Application Number : 23760

Regulatory Info : Prescription

Registration Country : Canada

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SUMITOMO PHARMA SWITZERLAND GMBH

Country
euroPLX 86 Munich
Not Confirmed
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SUMITOMO PHARMA SWITZERLAND GMBH

Country
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euroPLX 86 Munich
Not Confirmed

NORETHINDRONE ACETATE

Brand Name : MYFEMBREE

Dosage Form : TABLET

Dosage Strength : 0.5MG

Packaging :

Approval Date :

Application Number : 2541742

Regulatory Info : Prescription

Registration Country : Canada

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