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01 3ACLIDINIUM BROMIDE
02 1ACLIDINIUM BROMIDE; FORMOTEROL FUMARATE
03 1Aclidinium
04 3Aclidinium Bromide
05 2Aclidinium Bromide; Formoterol Fumarate Dihydrate
06 3Aclidinium bromide
07 7CICLESONIDE
08 5Ciclesonide
09 2Ciklesonid
10 2DIGOXIN
11 1FERUMOXIDES
12 1FERUMOXSIL
13 3FERUMOXYTOL
14 1FORMOTEROL FUMARATE DIHYDRATE
15 2Formoterol Fumarate Dihydrate; Aclidinium Bromide
16 2Formoterol; Aclidinium bromide
17 4LOVASTATIN
18 8NISOLDIPINE
19 2OMEPRAZOLE MAGNESIUM
20 1RILUZOLE
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01 2AMAG PHARMS INC
02 26COVIS
03 6COVIS PHARMA GMBH
04 2Covis Pharma Europe B.V.
05 15Covis Pharma Europe Bv
06 3Covis Pharma Gmbh
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01 2AEROSOL, METERED DOSE
02 2AEROSOL, METERED;INHALATION
03 1AEROSOL, METERED;NASAL
04 2FOR SUSPENSION, DELAYED RELEASE;ORAL
05 3INJECTABLE;INJECTION
06 2Inhalation Aerosol
07 9Inhalation Powder
08 2Inhalation Spray
09 2Inhalation aerosol, solution
10 3POWDER (METERED DOSE)
11 2POWDER, METERED;INHALATION
12 4Powder For Inhalation
13 3SOLUTION;INTRAVENOUS
14 1SPRAY, METERED DOSE
15 1SPRAY, METERED;NASAL
16 1SUSPENSION;ORAL
17 1Solution For Inhalation In Pressurized Container
18 12TABLET, EXTENDED RELEASE;ORAL
19 1TABLET;ORAL
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01 10.037MG/INH
02 10.05MG/SPRAY
03 10.08MG/INH
04 10.16MG/INH
05 10.1MG/ML
06 10.25MG/ML
07 10.4MG/INH
08 10.4MG/INH;0.012MG/INH
09 1100MCG/ACT
10 110MG
11 110MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
12 112MCG/ACT
13 1160 microg/dose
14 1160MCG
15 2160mcg/dose
16 117MG
17 1200MCG/ACT
18 120MG
19 120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
20 125.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
21 130MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
22 1322MCG
23 5322mcg
24 2340 mcg; 12 mcg
25 2340MCG; 12 MCG
26 2340mcg;12mcg
27 134MG
28 1375mcg
29 2400MCG/ACT
30 140MG
31 140MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
32 150MCG/ACT
33 150MG
34 160MG
35 18.5MG
36 180 microg/dose
37 280mcg/dose
38 1EQ 0.175MG IRON/ML
39 1EQ 10MG BASE/PACKET
40 1EQ 11.2MG IRON/ML
41 1EQ 2.5MG BASE/PACKET
42 1EQ 300MG IRON/10ML (EQ 30MG IRON/ML)
43 2EQ 510MG IRON/17ML (EQ 30MG IRON/ML)
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01 6Canada
02 5Moldova
03 2Norway
04 4Spain
05 6Sweden
06 3Switzerland
07 28USA
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Regulatory Info : Allowed
Registration Country : Switzerland
Dosage Form : Powder For Inhalation
Brand Name : Eklira Genuair
Dosage Strength : 375mcg
Packaging :
Approval Date : 2013-04-25
Application Number : 62590
Regulatory Info : Allowed
Registration Country : Switzerland

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Regulatory Info : RX
Registration Country : USA
Dosage Form : POWDER, METERED;INHALATI...
Brand Name : TUDORZA PRESSAIR
Dosage Strength : 0.4MG/INH
Packaging :
Approval Date : 2012-07-23
Application Number : 202450
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Inhalation Powder
Brand Name : Bretaris Genuair
Dosage Strength : 322mcg
Packaging :
Approval Date : 2012-07-20
Application Number : 20120218000051
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Inhalation Powder
Brand Name : Eklira Genuair
Dosage Strength : 322mcg
Packaging :
Approval Date : 2012-07-20
Application Number : 20110824000057
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Authorized
Registration Country : Spain
Dosage Form : Powder For Inhalation
Brand Name : Eklira Genuair
Dosage Strength : 322MCG
Packaging :
Approval Date : 2012-09-11
Application Number : 12778002
Regulatory Info : Authorized
Registration Country : Spain

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Regulatory Info : Prescription
Registration Country : Canada
Dosage Form : POWDER (METERED DOSE)
Brand Name : TUDORZA GENUAIR
Dosage Strength : 400MCG/ACT
Packaging :
Approval Date :
Application Number : 2409720
Regulatory Info : Prescription
Registration Country : Canada

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Regulatory Info : Prescription
Registration Country : Canada
Dosage Form : POWDER (METERED DOSE)
Brand Name : DUAKLIR GENUAIR
Dosage Strength : 400MCG/ACT
Packaging : 60 DOSES
Approval Date :
Application Number : 2439530
Regulatory Info : Prescription
Registration Country : Canada

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Regulatory Info :
Registration Country : Moldova
Dosage Form : Inhalation Powder
Brand Name : Bretaris® Genuair®
Dosage Strength : 322mcg
Packaging :
Approval Date : 27-12-2019
Application Number :
Regulatory Info :
Registration Country : Moldova

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Regulatory Info :
Registration Country : Moldova
Dosage Form : Inhalation Powder
Brand Name : Bretaris® Genuair®
Dosage Strength : 322mcg
Packaging :
Approval Date : 27-12-2019
Application Number :
Regulatory Info :
Registration Country : Moldova

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Regulatory Info :
Registration Country : Moldova
Dosage Form : Inhalation Powder
Brand Name : Bretaris® Genuair®
Dosage Strength : 322mcg
Packaging :
Approval Date : 27-12-2019
Application Number :
Regulatory Info :
Registration Country : Moldova
