Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
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01 1Sanofi
02 4AbbVie Inc
03 3Orion Corporation
04 10Alfred E Tiefenbacher GmbH
05 12care4 ApS
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07 4ANGITA PHARMA INC.
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18 3Bluefish Pharmaceuticals AB
19 7Chartwell Pharmaceuticals llc
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22 6Epic Pharma. LLC.
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26 7H. Lundbeck AS
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56 7Viatris
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01 4CAPSULE;ORAL
02 35FILM COATED PILL
03 10Film Coated Tablet
04 6SOLUTION;ORAL
05 7TAB
06 57TABLET
07 3TABLET, ORALLY DISINTEGRATING;ORAL
08 1TABLET; ORALLY DISINTEGRATING
09 81TABLET;ORAL
10 8Tablet
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01 59DISCN
02 10Generic
03 3Generic CTD, BE
04 1Originator
05 6Prescription
06 35RX
07 10Registered in EU
08 88Blank
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01 3AG-CITALOPRAM
02 1AG-CITALOPRAM TABLETS
03 2APO-CITALOPRAM
04 2AURO-CITALOPRAM
05 1Arrow Citalopram 20mg
06 1Arrow Citalopram 40mg
07 5CELEXA
08 1CELEXA 20 MG
09 1CELEXA 40 MG
10 9CITALOPRAM
11 1CITALOPRAM - 10
12 1CITALOPRAM - 20
13 1CITALOPRAM - 40
14 90CITALOPRAM HYDROBROMIDE
15 1CITALOPRESS 20
16 1CITALOPRESS 40
17 1CTP 30
18 2Cipramil
19 1Cipramil 20mg
20 3Citaloc
21 1Citalopram 2care4
22 3Citalopram Actavis
23 3Citalopram Bluefish
24 2Citalopram CNSpharma
25 4Citalopram Jubilant
26 4Citalopram Mylan
27 4Citalopram Orifarm
28 3Citalopram Orion
29 4Citalopram Sandoz
30 3Citalopram Teva
31 2Citalopram Vitabalans
32 1Citalopram-Winthrop 20 mg
33 1Citatrio
34 1DRL Citalopram 20
35 1DRL Citalopram 40
36 1Lopram 10
37 1Lopram 20
38 1Lopram 40
39 3M-CITALOPRAM
40 3MAR-CITALOPRAM
41 3MINT-CITALOPRAM
42 3NAT-CITALOPRAM
43 3NATCO-CITALOPRAM
44 3NRA-CITALOPRAM
45 6PMS-CITALOPRAM
46 3RIVA-CITALOPRAM
47 1Recita 20 mg
48 3TEVA-CITALOPRAM
49 13Blank
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01 53Canada
02 10Germany
03 9India
04 2Iran
05 1Pakistan
06 7South Africa
07 35Sweden
08 95USA
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Citalopram-Winthrop 20 mg
Dosage Form : TAB
Dosage Strength : 20mg
Packaging : 30X1mg
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Regulatory Info : RX
Registration Country : USA
Brand Name : CELEXA
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 2000-04-27
Application Number : 20822
Regulatory Info : RX
Registration Country : USA
Regulatory Info :
Registration Country : Sweden
Brand Name : Citalopram Orion
Dosage Form : FILM COATED PILL
Dosage Strength : 10 MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info : Registered in EU
Registration Country : Germany
Brand Name :
Dosage Form : Film Coated Tablet
Dosage Strength : 10MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Registered in EU
Registration Country : Germany
Regulatory Info : RX
Registration Country : USA
Brand Name : CELEXA
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 20MG BASE
Packaging :
Approval Date : 1998-07-17
Application Number : 20822
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : CELEXA
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 40MG BASE
Packaging :
Approval Date : 1998-07-17
Application Number : 20822
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CELEXA
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 60MG BASE
Packaging :
Approval Date : 1998-07-17
Application Number : 20822
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info :
Registration Country : Sweden
Brand Name : Citalopram Orion
Dosage Form : FILM COATED PILL
Dosage Strength : 20 MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
Brand Name : Citalopram Orion
Dosage Form : FILM COATED PILL
Dosage Strength : 40 MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info : Registered in EU
Registration Country : Germany
Brand Name :
Dosage Form : Film Coated Tablet
Dosage Strength : 20MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Registered in EU
Registration Country : Germany
Regulatory Info : Registered in EU
Registration Country : Germany
Brand Name :
Dosage Form : Film Coated Tablet
Dosage Strength : 30MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Registered in EU
Registration Country : Germany
Regulatory Info : Registered in EU
Registration Country : Germany
Brand Name :
Dosage Form : Film Coated Tablet
Dosage Strength : 40MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Registered in EU
Registration Country : Germany
Regulatory Info : Registered in EU
Registration Country : Germany
Brand Name :
Dosage Form : Film Coated Tablet
Dosage Strength : 60MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Registered in EU
Registration Country : Germany
Regulatory Info : Registered in EU
Registration Country : Germany
Brand Name :
Dosage Form : Film Coated Tablet
Dosage Strength : 10MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Registered in EU
Registration Country : Germany
Regulatory Info : Registered in EU
Registration Country : Germany
Brand Name :
Dosage Form : Film Coated Tablet
Dosage Strength : 20MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Registered in EU
Registration Country : Germany
Regulatory Info : Registered in EU
Registration Country : Germany
Brand Name :
Dosage Form : Film Coated Tablet
Dosage Strength : 30MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Registered in EU
Registration Country : Germany
Regulatory Info : Registered in EU
Registration Country : Germany
Brand Name :
Dosage Form : Film Coated Tablet
Dosage Strength : 40MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Registered in EU
Registration Country : Germany
Regulatory Info : Registered in EU
Registration Country : Germany
Brand Name :
Dosage Form : Film Coated Tablet
Dosage Strength : 60MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Registered in EU
Registration Country : Germany
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CITALOPRAM HYDROBROMIDE
Dosage Form : TABLET, ORALLY DISINTEGRATING;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 2005-12-20
Application Number : 21763
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CELEXA
Dosage Form : SOLUTION;ORAL
Dosage Strength : EQ 10MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1999-12-22
Application Number : 21046
Regulatory Info : DISCN
Registration Country : USA