01 1ALTAMED PHARMA
02 1ANGITA PHARMA INC.
03 2APOTEX INC
04 2AURO PHARMA INC
05 1BIOMED PHARMA
06 1FRESENIUS KABI CANADA LTD
07 1GENERIC MEDICAL PARTNERS INC
08 4JAMP PHARMA CORPORATION
09 1LABORATOIRE RIVA INC.
10 1MANTRA PHARMA INC
11 1MARCAN PHARMACEUTICALS INC
12 1MINT PHARMACEUTICALS INC
13 1NORA PHARMA INC
14 2Neogen N.V.
15 1PHARMASCIENCE INC
16 1PRO DOC LIMITEE
17 4Pharmascience Inc.
18 3SANDOZ CANADA INCORPORATED
19 2SANIS HEALTH INC
20 2SIVEM PHARMACEUTICALS ULC
21 1SUN PHARMA CANADA INC
22 2TAKEDA CANADA INC
23 2TEVA CANADA LIMITED
01 22PANTOPRAZOLE (PANTOPRAZOLE SODIUM SESQUIHYDRATE)
02 10PANTOPRAZOLE (PANTOPRAZOLE SODIUM)
03 2PANTOPRAZOLE SODIUM
04 2Pantoprazole
05 2Pantoprazole Sodium Sesquihydrate
01 1LYOPHYLIZED POWDER FOR INJECTION
02 6POWDER FOR SOLUTION
03 1SOLUTION FOR INFUSION
04 28TABLET (DELAYED-RELEASE)
05 2TABLET (ENTERIC-COATED)
01 1AG-PANTOPRAZOLE SODIUM
02 2APO-PANTOPRAZOLE
03 1AURO-PANTOPRAZOLE
04 1BIO-PANTOPRAZOLE
05 2JAMP PANTOPRAZOLE SODIUM
06 1JAMP-PANTOPRAZOLE
07 1M-PANTOPRAZOLE
08 1MAR-PANTOPRAZOLE
09 1MINT-PANTOPRAZOLE
10 1NRA-PANTOPRAZOLE
11 2PANTOLOC
12 8PANTOPRAZOLE
13 2PANTOPRAZOLE FOR INJECTION
14 3PANTOPRAZOLE SODIUM FOR INJECTION
15 4PMS-PANTOPRAZOLE
16 2SANDOZ PANTOPRAZOLE
17 1TARO-PANTOPRAZOLE
18 2TEVA-PANTOPRAZOLE
19 2Blank
Regulatory Info : Generic
Registration Country : Canada
Brand Name :
Dosage Form : LYOPHYLIZED POWDER FOR INJECTION
Dosage Strength : 40MG
Packaging : Glass Vial
Approval Date :
Application Number : 79197
Regulatory Info : Generic
Registration Country : Canada
Regulatory Info : Generic DCP completed
Registration Country : Canada
Brand Name :
Dosage Form : SOLUTION FOR INFUSION
Dosage Strength : 10MG/ML
Packaging : Glass Vial
Approval Date :
Application Number :
Regulatory Info : Generic DCP completed
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : PMS-PANTOPRAZOLE
Dosage Form : TABLET (DELAYED-RELEASE)
Dosage Strength : 20MG
Packaging : 100
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : PMS-PANTOPRAZOLE
Dosage Form : TABLET (DELAYED-RELEASE)
Dosage Strength : 40MG
Packaging : 100/500
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Pantoprazole Sodium Sesquihydrate
Brand Name : PANTOPRAZOLE
Dosage Form : TABLET (DELAYED-RELEASE)
Dosage Strength : 40MG
Packaging : 100/500
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Pantoprazole Sodium Sesquihydrate
Brand Name : PMS-PANTOPRAZOLE
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 40MG
Packaging : 10ML
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
PANTOPRAZOLE (PANTOPRAZOLE SODIUM)
Brand Name : PANTOPRAZOLE
Dosage Form : TABLET (DELAYED-RELEASE)
Dosage Strength : 40MG
Packaging : 100/500
Approval Date :
Application Number : 2318695
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
PANTOPRAZOLE (PANTOPRAZOLE SODIUM)
Brand Name : PANTOLOC
Dosage Form : TABLET (ENTERIC-COATED)
Dosage Strength : 40MG
Packaging : 7/100
Approval Date :
Application Number : 2229453
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
PANTOPRAZOLE (PANTOPRAZOLE SODIUM)
Brand Name : PANTOLOC
Dosage Form : TABLET (ENTERIC-COATED)
Dosage Strength : 20MG
Packaging : 100
Approval Date :
Application Number : 2241804
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
PANTOPRAZOLE (PANTOPRAZOLE SODIUM SESQUIHYDRATE)
Brand Name : TEVA-PANTOPRAZOLE
Dosage Form : TABLET (DELAYED-RELEASE)
Dosage Strength : 20MG
Packaging :
Approval Date :
Application Number : 2285479
Regulatory Info : Prescription
Registration Country : Canada
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