01 1ACCORD HEALTHCARE INC
02 1ANGITA PHARMA INC.
03 3APOTEX INC
04 3AURO PHARMA INC
05 1BIOMED PHARMA
06 3JAMP PHARMA CORPORATION
07 1LABORATOIRE RIVA INC.
08 1MANTRA PHARMA INC
09 1MARCAN PHARMACEUTICALS INC
10 3MINT PHARMACEUTICALS INC
11 3NATCO PHARMA (CANADA) INC
12 1NORA PHARMA INC
13 4ORGANON CANADA INC.
14 3PHARMASCIENCE INC
15 3PRO DOC LIMITEE
16 3Pharmascience Inc.
17 4SANDOZ CANADA INCORPORATED
18 2SANIS HEALTH INC
19 3SIVEM PHARMACEUTICALS ULC
20 1SUN PHARMA CANADA INC
21 3TEVA CANADA LIMITED
01 45MONTELUKAST (MONTELUKAST SODIUM)
02 3MONTELUKAST SODIUM
01 2GRANULES
02 21TABLET
03 25TABLET (CHEWABLE)
01 1ACH-MONTELUKAST
02 1AG-MONTELUKAST
03 3APO-MONTELUKAST
04 1AURO-MONTELUKAST
05 2AURO-MONTELUKAST CHEWABLE TABLET
06 1BIO-MONTELUKAST
07 2JAMP MONTELUKAST CHEWABLE TABLETS
08 1JAMP-MONTELUKAST
09 1M-MONTELUKAST
10 1MAR-MONTELUKAST
11 3MINT-MONTELUKAST
12 8MONTELUKAST
13 3NAT-MONTELUKAST
14 1NRA-MONTELUKAST
15 4PMS-MONTELUKAST
16 2PMS-MONTELUKAST FC
17 1RIVA-MONTELUKAST FC
18 4SANDOZ MONTELUKAST
19 4SINGULAIR
20 1TARO-MONTELUKAST
21 3TEVA-MONTELUKAST
Regulatory Info : Prescription
Registration Country : Canada
MONTELUKAST (MONTELUKAST SODIUM)
Brand Name : AURO-MONTELUKAST
Dosage Form : TABLET
Dosage Strength : 10MG
Packaging : Oct-30
Approval Date :
Application Number : 2401274
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : PMS-MONTELUKAST
Dosage Form : TABLET (CHEWABLE)
Dosage Strength : 4MG
Packaging : 30/100
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : PMS-MONTELUKAST
Dosage Form : TABLET (CHEWABLE)
Dosage Strength : 5MG
Packaging : 30/100
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : PMS-MONTELUKAST FC
Dosage Form : TABLET
Dosage Strength : 10MG
Packaging : 30/100
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
MONTELUKAST (MONTELUKAST SODIUM)
Brand Name : SANDOZ MONTELUKAST
Dosage Form : TABLET
Dosage Strength : 10MG
Packaging : 28/100/250
Approval Date :
Application Number : 2328593
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
MONTELUKAST (MONTELUKAST SODIUM)
Brand Name : SINGULAIR
Dosage Form : TABLET (CHEWABLE)
Dosage Strength : 5MG
Packaging :
Approval Date :
Application Number : 2238216
Regulatory Info : Prescription
Registration Country : Canada
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : Prescription
Registration Country : Canada
MONTELUKAST (MONTELUKAST SODIUM)
Brand Name : SINGULAIR
Dosage Form : TABLET
Dosage Strength : 10MG
Packaging :
Approval Date :
Application Number : 2238217
Regulatory Info : Prescription
Registration Country : Canada
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : Prescription
Registration Country : Canada
MONTELUKAST (MONTELUKAST SODIUM)
Brand Name : SINGULAIR
Dosage Form : TABLET (CHEWABLE)
Dosage Strength : 4MG
Packaging :
Approval Date :
Application Number : 2243602
Regulatory Info : Prescription
Registration Country : Canada
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : Prescription
Registration Country : Canada
MONTELUKAST (MONTELUKAST SODIUM)
Brand Name : SINGULAIR
Dosage Form : GRANULES
Dosage Strength : 4MG/SACHET
Packaging :
Approval Date :
Application Number : 2247997
Regulatory Info : Prescription
Registration Country : Canada
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : Prescription
Registration Country : Canada
MONTELUKAST (MONTELUKAST SODIUM)
Brand Name : RIVA-MONTELUKAST FC
Dosage Form : TABLET
Dosage Strength : 10MG
Packaging : 30/100
Approval Date :
Application Number : 2398826
Regulatory Info : Prescription
Registration Country : Canada
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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