01 3ACLIDINIUM BROMIDE
02 1ACLIDINIUM BROMIDE; FORMOTEROL FUMARATE
03 3Aclidinium
04 5Aclidinium Bromide
05 4Aclidinium Bromide; Formoterol Fumarate Dihydrate
06 2Aclidinium Bromide; Formoterol fumarate dihydrate
07 5Aclidinium bromide
08 7CICLESONIDE
09 9Ciclesonide
10 2DIGOXIN
11 1FERUMOXIDES
12 1FERUMOXSIL
13 3FERUMOXYTOL
14 1FORMOTEROL FUMARATE DIHYDRATE
15 2Formoterol Fumarate Dihydrate; Aclidinium Bromide
16 2Formoterol; Aclidinium
17 2Formoterol; Aclidinium bromide
18 4LOVASTATIN
19 8NISOLDIPINE
20 2OMEPRAZOLE MAGNESIUM
21 1RILUZOLE
01 2AMAG PHARMS INC
02 26COVIS
03 6COVIS PHARMA GMBH
04 10Covis Pharma Europe B.V.
05 6Covis Pharma Europe BV
06 15Covis Pharma Europe Bv
07 3Covis Pharma Gmbh
01 2AEROSOL, METERED DOSE
02 2AEROSOL, METERED;INHALATION
03 1AEROSOL, METERED;NASAL
04 2FOR SUSPENSION, DELAYED RELEASE;ORAL
05 3INJECTABLE;INJECTION
06 4Inhalation Aerosol
07 21Inhalation Powder
08 4Inhalation Spray
09 3POWDER (METERED DOSE)
10 2POWDER, METERED;INHALATION
11 4Powder For Inhalation
12 3SOLUTION;INTRAVENOUS
13 1SPRAY, METERED DOSE
14 1SPRAY, METERED;NASAL
15 1SUSPENSION;ORAL
16 1Solution For Inhalation In Pressurized Container
17 12TABLET, EXTENDED RELEASE;ORAL
18 1TABLET;ORAL
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11 110MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 1118mcg/dose; 340mcg/dose
13 1118mcg; 340mcg
14 112MCG/ACT
15 1160 mcg/dose
16 1160MCG
17 3160mcg/dose
18 117MG
19 1200MCG/ACT
20 120MG
21 120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
22 125.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
23 130MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
24 1322MCG
25 9322mcg
26 1322mcg/actuation
27 1322mcg/inh
28 2340 mcg; 12 mcg
29 2340MCG; 12 MCG
30 4340mcg; 12mcg
31 2340mcg;12mcg
32 134MG
33 1375mcg
34 2400MCG/ACT
35 140MG
36 140MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
37 150MCG/ACT
38 150MG
39 160MG
40 18.5MG
41 480mcg/dose
42 1EQ 0.175MG IRON/ML
43 1EQ 10MG BASE/PACKET
44 1EQ 11.2MG IRON/ML
45 1EQ 2.5MG BASE/PACKET
46 1EQ 300MG IRON/10ML (EQ 30MG IRON/ML)
47 2EQ 510MG IRON/17ML (EQ 30MG IRON/ML)
01 6Canada
02 6Denmark
03 4Estonia
04 5Moldova
05 6Norway
06 4Spain
07 6Sweden
08 3Switzerland
09 28USA
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
Regulatory Info : Prescription
Registration Country : Estonia
Dosage Form : Inhalation Powder
Brand Name : Bretaris Genuair
Dosage Strength : 322mcg/actuation
Packaging :
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Estonia
Regulatory Info : Prescription
Registration Country : Estonia
Dosage Form : Inhalation Powder
Brand Name : Eklira Genuair
Dosage Strength : 322mcg/inh
Packaging :
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Estonia
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
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
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
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
Regulatory Info : Marketed
Registration Country : Norway
Dosage Form : Inhalation Powder
Brand Name : Eklira Genuair
Dosage Strength : 322mcg
Packaging :
Approval Date :
Application Number :
Regulatory Info : Marketed
Registration Country : Norway
Regulatory Info : Marketed
Registration Country : Norway
Dosage Form : Inhalation Powder
Brand Name : Eklira Genuair
Dosage Strength : 322mcg
Packaging :
Approval Date :
Application Number :
Regulatory Info : Marketed
Registration Country : Norway
Regulatory Info : Authorized
Registration Country : Spain
Dosage Form : Powder For Inhalation
Brand Name : Eklira Genuair
Dosage Strength : 322MCG
Packaging :
Approval Date : 11-09-2012
Application Number : 12778002
Regulatory Info : Authorized
Registration Country : Spain
