01 1ACETYLSALICYLIC ACID
02 3AMLODIPINE (AMLODIPINE BESYLATE)
03 2DULOXETINE (DULOXETINE HYDROCHLORIDE)
04 1PANTOPRAZOLE (PANTOPRAZOLE SODIUM SESQUIHYDRATE)
05 3PAROXETINE (PAROXETINE HYDROCHLORIDE HEMIHYDRATE)
06 4PREGABALIN
07 3SERTRALINE (SERTRALINE HYDROCHLORIDE)
08 1SILDENAFIL (SILDENAFIL CITRATE)
09 2ZOPICLONE
01 7CAPSULE
02 2CAPSULE (DELAYED RELEASE)
03 9TABLET
04 1TABLET (CHEWABLE)
05 1TABLET (DELAYED-RELEASE)
01 2100MG
02 210MG
03 1150MG
04 12.5MG
05 120MG
06 225MG
07 230MG
08 140MG
09 250MG
10 25MG
11 160MG
12 17.5MG
13 175MG
14 180MG
01 3AMLODIPINE
02 1ASA 80MG
03 2DULOXETINE
04 1PANTOPRAZOLE
05 3PAROXETINE
06 4PREGABALIN
07 3SERTRALINE
08 1SILDENAFIL
09 2ZOPICLONE
Regulatory Info :
Registration Country : Canada
PAROXETINE (PAROXETINE HYDROCHLORIDE HEMIHYDRATE)
Dosage Form : TABLET
Dosage Strength : 10MG
Packaging : (3X10)/100/500
Brand Name : PAROXETINE
Approval Date :
Application Number : 2477823
Regulatory Info :
Registration Country : Canada
Regulatory Info :
Registration Country : Canada
PAROXETINE (PAROXETINE HYDROCHLORIDE HEMIHYDRATE)
Dosage Form : TABLET
Dosage Strength : 20MG
Packaging : (3X10)/100/500
Brand Name : PAROXETINE
Approval Date :
Application Number : 2477831
Regulatory Info :
Registration Country : Canada
Regulatory Info :
Registration Country : Canada
PAROXETINE (PAROXETINE HYDROCHLORIDE HEMIHYDRATE)
Dosage Form : TABLET
Dosage Strength : 30MG
Packaging : (3X10)/100/500
Brand Name : PAROXETINE
Approval Date :
Application Number : 2477858
Regulatory Info :
Registration Country : Canada
Regulatory Info :
Registration Country : Canada
DULOXETINE (DULOXETINE HYDROCHLORIDE)
Dosage Form : CAPSULE (DELAYED RELEASE)
Dosage Strength : 30MG
Packaging :
Brand Name : DULOXETINE
Approval Date :
Application Number : 2481952
Regulatory Info :
Registration Country : Canada
Regulatory Info :
Registration Country : Canada
DULOXETINE (DULOXETINE HYDROCHLORIDE)
Dosage Form : CAPSULE (DELAYED RELEASE)
Dosage Strength : 60MG
Packaging :
Brand Name : DULOXETINE
Approval Date :
Application Number : 2481960
Regulatory Info :
Registration Country : Canada
Regulatory Info :
Registration Country : Canada
AMLODIPINE (AMLODIPINE BESYLATE)
Dosage Form : TABLET
Dosage Strength : 2.5MG
Packaging :
Brand Name : AMLODIPINE
Approval Date :
Application Number : 2490781
Regulatory Info :
Registration Country : Canada
Regulatory Info :
Registration Country : Canada
AMLODIPINE (AMLODIPINE BESYLATE)
Dosage Form : TABLET
Dosage Strength : 5MG
Packaging :
Brand Name : AMLODIPINE
Approval Date :
Application Number : 2490803
Regulatory Info :
Registration Country : Canada
Regulatory Info :
Registration Country : Canada
AMLODIPINE (AMLODIPINE BESYLATE)
Dosage Form : TABLET
Dosage Strength : 10MG
Packaging :
Brand Name : AMLODIPINE
Approval Date :
Application Number : 2490811
Regulatory Info :
Registration Country : Canada
Regulatory Info :
Registration Country : Canada
Dosage Form : TABLET (CHEWABLE)
Dosage Strength : 80MG
Packaging :
Brand Name : ASA 80MG
Approval Date :
Application Number : 2497115
Regulatory Info :
Registration Country : Canada
Regulatory Info :
Registration Country : Canada
PANTOPRAZOLE (PANTOPRAZOLE SODIUM SESQUIHYDRATE)
Dosage Form : TABLET (DELAYED-RELEASE)
Dosage Strength : 40MG
Packaging : 100/500
Brand Name : PANTOPRAZOLE
Approval Date :
Application Number : 2469138
Regulatory Info :
Registration Country : Canada
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