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01 2BETHANECHOL CHLORIDE
02 10CENOBAMATE
03 3CLIOQUINOL
04 1CLODRONATE DISODIUM
05 1DICLOFENAC SODIUM
06 1DIPHENHYDRAMINE HYDROCHLORIDE
07 1ESTRADIOL
08 3ESTRADIOL (ESTRADIOL HEMIHYDRATE)
09 2FLUMETHASONE PIVALATE
10 1HYDROCORTISONE
11 2LABETALOL HYDROCHLORIDE
12 1METHIMAZOLE
13 5METHYLPHENIDATE HYDROCHLORIDE
14 2NALOXEGOL (NALOXEGOL OXALATE)
15 1NERATINIB (NERATINIB MALEATE)
16 1NETUPITANT
17 1NORETHINDRONE ACETATE
18 2PALONOSETRON (PALONOSETRON HYDROCHLORIDE)
19 1PIZOTIFEN (PIZOTIFEN MALATE)
20 1PROGESTERONE
21 2RELUGOLIX
22 3RIVASTIGMINE
23 5RIVASTIGMINE (RIVASTIGMINE HYDROGEN TARTRATE)
24 1TENAPANOR (TENAPANOR HYDROCHLORIDE)
25 3TRIPTORELIN (TRIPTORELIN PAMOATE)
26 2WHITE PETROLATUM
27 2ZINC OXIDE
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01 9CAPSULE
02 5CAPSULE (DELAYED AND EXTENDED RELEASE)
03 4CREAM
04 2DROPS
05 2INSERT
06 2KIT
07 4OINTMENT
08 3PATCH
09 3POWDER FOR SUSPENSION, SUSTAINED-RELEASE
10 3SOLUTION
11 23TABLET
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01 10.02%/W/V
02 10.02%/W/W
03 10.25MG/5ML
04 20.5MG
05 11%/W/V
06 11%/W/W
07 11.5%/W/W
08 11.5MG
09 5100MG
10 110MCG/INSERT
11 210MG
12 111.25MG/VIAL
13 312.5MG
14 1120MG
15 113.3MG/24HOUR
16 115%/W/W
17 1150MG
18 31MG
19 2200MG
20 120MG
21 122.5MG/VIAL
22 425MG
23 12MG/ML
24 23%/W/W
25 13.75MG/VIAL
26 1300MG
27 13MG
28 14.5MG
29 14.6MG/24HOUR
30 140%/W/W
31 1400MG
32 340MG
33 147%/W/W
34 14MCG/INSERT
35 450MG
36 160MG
37 169%/W/W
38 16MG
39 180MG
40 19.5MG/24HOUR
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01 2AKYNZEO
02 1ALOXI
03 2BIJUVA
04 1CLASTEON
05 2DUVOID
06 5EXELON
07 1EXELON PATCH 10
08 1EXELON PATCH 15
09 1EXELON PATCH 5
10 1IBSRELA
11 2IMVEXXY
12 5JORNAY PM
13 2LOCACORTEN VIOFORM
14 2LOCACORTEN VIOFORM EARDROPS
15 2MOVANTIK
16 3MYFEMBREE
17 1NERLYNX
18 1ORGOVYX
19 1PENNSAID
20 1SANDOMIGRAN DS
21 1TAPAZOLE
22 2TRANDATE
23 3TRELSTAR
24 1UNISOM
25 2VIOFORM HYDROCORTISONE
26 10XCOPRI
27 2ZINCOFAX
28 2ZINCOFAX EXTRA STRENGTH
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Regulatory Info : Prescription
Registration Country : Canada
Dosage Form : TABLET
Dosage Strength : 25MG
Packaging :
Brand Name : DUVOID
Approval Date :
Application Number : 1947931
Regulatory Info : Prescription
Registration Country : Canada

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Regulatory Info : Prescription
Registration Country : Canada
Dosage Form : TABLET
Dosage Strength : 10MG
Packaging :
Brand Name : DUVOID
Approval Date :
Application Number : 1947958
Regulatory Info : Prescription
Registration Country : Canada

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Regulatory Info : Prescription
Registration Country : Canada
Dosage Form : TABLET
Dosage Strength : 12.5MG
Packaging :
Brand Name : XCOPRI
Approval Date :
Application Number : 2538652
Regulatory Info : Prescription
Registration Country : Canada

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Regulatory Info : Prescription
Registration Country : Canada
Dosage Form : TABLET
Dosage Strength : 25MG
Packaging :
Brand Name : XCOPRI
Approval Date :
Application Number : 2538660
Regulatory Info : Prescription
Registration Country : Canada

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Regulatory Info : Prescription
Registration Country : Canada
Dosage Form : TABLET
Dosage Strength : 50MG
Packaging :
Brand Name : XCOPRI
Approval Date :
Application Number : 2538725
Regulatory Info : Prescription
Registration Country : Canada

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Regulatory Info : Prescription
Registration Country : Canada
Dosage Form : TABLET
Dosage Strength : 100MG
Packaging :
Brand Name : XCOPRI
Approval Date :
Application Number : 2538733
Regulatory Info : Prescription
Registration Country : Canada

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Regulatory Info : Prescription
Registration Country : Canada
Dosage Form : TABLET
Dosage Strength : 150MG
Packaging :
Brand Name : XCOPRI
Approval Date :
Application Number : 2538741
Regulatory Info : Prescription
Registration Country : Canada

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Regulatory Info : Prescription
Registration Country : Canada
Dosage Form : TABLET
Dosage Strength : 200MG
Packaging :
Brand Name : XCOPRI
Approval Date :
Application Number : 2538768
Regulatory Info : Prescription
Registration Country : Canada

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Regulatory Info : Prescription
Registration Country : Canada
Dosage Form : KIT
Dosage Strength : 25MG
Packaging :
Brand Name : XCOPRI
Approval Date :
Application Number : 2538776
Regulatory Info : Prescription
Registration Country : Canada

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Regulatory Info : Prescription
Registration Country : Canada
Dosage Form : KIT
Dosage Strength : 12.5MG
Packaging :
Brand Name : XCOPRI
Approval Date :
Application Number : 2538776
Regulatory Info : Prescription
Registration Country : Canada
