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01 1Anastrozol
02 9Anastrozole
03 1BISMUTH SUBCITRATE POTASSIUM; METRONIDAZOLE; TETRACYCLINE HYDROCHLORIDE
04 1Betahistine Dimesilate
05 9Bicalutamide
06 3Bikalutamid
07 1Clothipine
08 4Hydrochlorothiazide
09 1METRONIDAZOLE
10 17Ponesimod
11 1Ponesimode
12 1TETRACYCLINE HYDROCHLORIDE
13 1Tetracycline Hydrochloride; Metronidazole; Bismuth Subcitrate
14 1bismuth oxide; Bismuth Subcitrate Potassium
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01 2Juvise Pharmaceuticals
02 2LABORATOIRES JUVISE PHARMACEUTICALS
03 2LABORATORIES JUVISE PHARMACEUTICALS
04 4LABORATORIES JUVISE' PHARMACEUTICALS
05 1LABS JUVISE
06 23Laboratoires Juvise Pharmaceuticals
07 17Laboratoires Juvisé Pharmaceuticals
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01 3CAPSULE
02 1CAPSULE;ORAL
03 2Capsule
04 32Film Coated Tablet
05 5Film-Coated Tablet
06 3Film-Coated Tablets
07 4Tablet
08 1Tablets
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01 11 mg
02 110MG
03 110mg
04 2125MG
05 112MG
06 1140MG; 125MG; 125 MG
07 1140MG;125MG;125MG
08 1150 mg
09 1150MG
10 5150mg
11 51MG
12 21mg
13 120MG
14 420mg
15 125 mg
16 125MG
17 225mg
18 12mg
19 13mg
20 240MG
21 150 mg
22 150MG
23 350mg
24 15mg
25 16mg
26 17mg
27 18mg
28 29mg
29 5Blank
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01 3Canada
02 12Denmark
03 5Estonia
04 1France
05 4Italy
06 7Norway
07 12Spain
08 6Sweden
09 1USA
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Regulatory Info : Marketed
Registration Country : Norway
Dosage Form : Film Coated Tablet
Brand Name : Arimidex
Dosage Strength : 1mg
Packaging :
Approval Date :
Application Number :
Regulatory Info : Marketed
Registration Country : Norway

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Regulatory Info :
Registration Country : Italy
Dosage Form : Film-Coated Tablets
Brand Name : ARIMIDEX
Dosage Strength : 1 mg
Packaging : 28 UNITS 1 MG - ORAL USE
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy

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Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Film Coated Tablet
Brand Name : Arimidex
Dosage Strength :
Packaging :
Approval Date : 12/04/1996
Application Number : 19960412000075
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Prescription
Registration Country : Estonia
Dosage Form : Film-Coated Tablet
Brand Name : Arimidex
Dosage Strength : 1mg
Packaging :
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Estonia

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Regulatory Info : Authorized
Registration Country : Spain
Dosage Form : Film Coated Tablet
Brand Name : Arimidex
Dosage Strength : 1MG
Packaging :
Approval Date : 21-12-2021
Application Number : 44579-14-06-2016IP
Regulatory Info : Authorized
Registration Country : Spain

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Regulatory Info : Authorized
Registration Country : Spain
Dosage Form : Film Coated Tablet
Brand Name : Arimidex
Dosage Strength : 1MG
Packaging :
Approval Date : 01-01-1997
Application Number : 61286
Regulatory Info : Authorized
Registration Country : Spain

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Regulatory Info : Authorized
Registration Country : Spain
Dosage Form : Film Coated Tablet
Brand Name : Arimidex
Dosage Strength : 1MG
Packaging :
Approval Date : 27-09-2019
Application Number : 2268001
Regulatory Info : Authorized
Registration Country : Spain

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Regulatory Info : Authorized
Registration Country : Spain
Dosage Form : Film Coated Tablet
Brand Name : Arimidex
Dosage Strength : 1MG
Packaging :
Approval Date : 22-10-2019
Application Number : 44-1296-97-C
Regulatory Info : Authorized
Registration Country : Spain

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Regulatory Info : Authorized
Registration Country : Spain
Dosage Form : Film Coated Tablet
Brand Name : Arimidex
Dosage Strength : 1MG
Packaging :
Approval Date : 03-04-2020
Application Number : 44579-14-06-2016
Regulatory Info : Authorized
Registration Country : Spain

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Regulatory Info : Prescription
Registration Country : Denmark
Dosage Form : Film Coated Tablet
Brand Name : Arimidex
Dosage Strength :
Packaging :
Approval Date : 20-09-1996
Application Number : 28101752195
Regulatory Info : Prescription
Registration Country : Denmark
