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01 1ABIRATERONE ACETATE
02 1ANASTROZOLE
03 2APIXABAN
04 2BENDAMUSTINE HYDROCHLORIDE
05 2BOSENTAN (BOSENTAN MONOHYDRATE)
06 2CETIRIZINE HYDROCHLORIDE
07 3CITALOPRAM (CITALOPRAM HYDROBROMIDE)
08 1ERIBULIN MESYLATE
09 3ERLOTINIB (ERLOTINIB HYDROCHLORIDE)
10 2ESCITALOPRAM (ESCITALOPRAM OXALATE)
11 3EVEROLIMUS
12 1GRANISETRON (GRANISETRON HYDROCHLORIDE)
13 2IMATINIB (IMATINIB MESYLATE)
14 4LANTHANUM (LANTHANUM CARBONATE DIHYDRATE)
15 6LENALIDOMIDE
16 1LETROZOLE
17 3MONTELUKAST (MONTELUKAST SODIUM)
18 2ONDANSETRON (ONDANSETRON HYDROCHLORIDE DIHYDRATE)
19 4OSELTAMIVIR (OSELTAMIVIR PHOSPHATE)
20 4POMALIDOMIDE
21 6PREGABALIN
22 2RIZATRIPTAN (RIZATRIPTAN BENZOATE)
23 3SITAGLIPTIN (SITAGLIPTIN PHOSPHATE MONOHYDRATE)
24 3SUNITINIB (SUNITINIB MALATE)
25 1TENOFOVIR DISOPROXIL FUMARATE
26 1TERIFLUNOMIDE
27 1ZOLMITRIPTAN
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01 22CAPSULE
02 2POWDER FOR SOLUTION
03 1POWDER FOR SUSPENSION
04 1SOLUTION
05 32TABLET
06 6TABLET (CHEWABLE)
07 2TABLET (ORALLY DISINTEGRATING)
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01 10.5MG/ML
02 11000MG
03 3100MG
04 1100MG/VIAL
05 710MG
06 112.5MG
07 1125MG
08 114MG
09 2150MG
10 115MG
11 31MG
12 52.5MG
13 420MG
14 1225MG
15 2250MG
16 525MG
17 125MG/VIAL
18 12MG
19 2300MG
20 130MG
21 13MG
22 1400MG
23 140MG
24 145MG
25 34MG
26 1500MG
27 350MG
28 55MG
29 162.5MG
30 16MG/ML
31 1750MG
32 275MG
33 18MG
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01 1NAT-ABIRATERONE
02 1NAT-ANASTROZOLE
03 2NAT-APIXABAN
04 2NAT-BENDAMUSTINE
05 2NAT-BOSENTAN
06 2NAT-CETIRIZINE
07 1NAT-ERIBULIN
08 3NAT-ERLOTINIB
09 3NAT-EVEROLIMUS
10 1NAT-GRANISETRON
11 2NAT-IMATINIB
12 4NAT-LANTHANUM
13 6NAT-LENALIDOMIDE
14 1NAT-LETROZOLE
15 3NAT-MONTELUKAST
16 2NAT-ONDANSETRON
17 4NAT-OSELTAMIVIR
18 4NAT-POMALIDOMIDE
19 6NAT-PREGABALIN
20 2NAT-RIZATRIPTAN ODT
21 3NAT-SITAGLIPTIN
22 3NAT-SUNITINIB
23 1NAT-TENOFOVIR
24 1NAT-TERIFLUNOMIDE
25 1NAT-ZOLMITRIPTAN
26 3NATCO-CITALOPRAM
27 2NATCO-ESCITALOPRAM
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Regulatory Info : PRESCRIPTION
Registration Country : Canada
Dosage Form : TABLET
Dosage Strength : 1MG
Packaging : 30
Brand Name : NAT-ANASTROZOLE
Approval Date :
Application Number : 2417855
Regulatory Info : PRESCRIPTION
Registration Country : Canada

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Regulatory Info : PRESCRIPTION
Registration Country : Canada
BOSENTAN (BOSENTAN MONOHYDRATE)
Dosage Form : TABLET
Dosage Strength : 62.5MG
Packaging : 06/10/1960
Brand Name : NAT-BOSENTAN
Approval Date :
Application Number : 2467984
Regulatory Info : PRESCRIPTION
Registration Country : Canada

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Regulatory Info : PRESCRIPTION
Registration Country : Canada
BOSENTAN (BOSENTAN MONOHYDRATE)
Dosage Form : TABLET
Dosage Strength : 125MG
Packaging : 4/14/60
Brand Name : NAT-BOSENTAN
Approval Date :
Application Number : 2467992
Regulatory Info : PRESCRIPTION
Registration Country : Canada

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Regulatory Info : PRESCRIPTION
Registration Country : Canada
Dosage Form : TABLET
Dosage Strength : 2.5MG
Packaging :
Brand Name : NAT-APIXABAN
Approval Date :
Application Number : 2492814
Regulatory Info : PRESCRIPTION
Registration Country : Canada

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Regulatory Info : PRESCRIPTION
Registration Country : Canada
Dosage Form : TABLET
Dosage Strength : 5MG
Packaging :
Brand Name : NAT-APIXABAN
Approval Date :
Application Number : 2492822
Regulatory Info : PRESCRIPTION
Registration Country : Canada

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Regulatory Info : PRESCRIPTION
Registration Country : Canada
Dosage Form : TABLET
Dosage Strength : 250MG
Packaging :
Brand Name : NAT-ABIRATERONE
Approval Date :
Application Number : 2494132
Regulatory Info : PRESCRIPTION
Registration Country : Canada

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Regulatory Info : NON-PRESCRIPTION DRUGS
Registration Country : Canada
Dosage Form : TABLET
Dosage Strength : 10MG
Packaging :
Brand Name : NAT-CETIRIZINE
Approval Date :
Application Number : 2496461
Regulatory Info : NON-PRESCRIPTION DRUGS
Registration Country : Canada

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Regulatory Info : PRESCRIPTION
Registration Country : Canada
Dosage Form : TABLET
Dosage Strength : 20MG
Packaging :
Brand Name : NAT-CETIRIZINE
Approval Date :
Application Number : 2496488
Regulatory Info : PRESCRIPTION
Registration Country : Canada

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Regulatory Info : PRESCRIPTION
Registration Country : Canada
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 25MG/VIAL
Packaging :
Brand Name : NAT-BENDAMUSTINE
Approval Date :
Application Number : 2496887
Regulatory Info : PRESCRIPTION
Registration Country : Canada

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Regulatory Info : PRESCRIPTION
Registration Country : Canada
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 100MG/VIAL
Packaging :
Brand Name : NAT-BENDAMUSTINE
Approval Date :
Application Number : 2496895
Regulatory Info : PRESCRIPTION
Registration Country : Canada
