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Athena Athena

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Cordenpharma's list of EU CTD Dossiers, Marketing Authorizations, In, Out Licensing Opportunities & Finished Dosage Formulations aggregated by PharmaCompass

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01 CARBOPLATIN (7)

02 CEFPROZIL (4)

03 ETOPOSIDE (1)

04 LOMUSTINE (4)

05 Propofol (1)

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01 CORDEN PHARMA (12)

02 CORDENPHARMA (4)

03 Corden Pharma Latina S.p.A (1)

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01 CAPSULE;ORAL (4)

02 FOR SUSPENSION;ORAL (2)

03 INJECTABLE;INJECTION (4)

04 INJECTABLE;INTRAVENOUS (4)

05 Propofol 200Mg 20Ml 5 Units Parenteral Use (1)

06 TABLET;ORAL (2)

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01 100MG (1)

02 10MG (1)

03 125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

04 150MG/15ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

05 150MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

06 20MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

07 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

08 250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

09 40MG (1)

10 450MG/45ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

11 450MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

12 5 VIALS EV 20 ml 10 mg/ml (1)

13 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

14 50MG/5ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

15 50MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

16 5MG (1)

17 600MG/60ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

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01 Italy (1)

02 USA (16)

URL Supplier Web Content
INJECTABLE;INJECTION
50MG/VIAL **Federal Re...
PARAPLATIN
USA
19880
1989-03-03
DISCN
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US
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URL Supplier Web Content
INJECTABLE;INJECTION
150MG/VIAL **Federal R...
PARAPLATIN
USA
19880
1989-03-03
DISCN
ASK
US
PHARMACOMPASS
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your Marketing & Sales content
URL Supplier Web Content
INJECTABLE;INJECTION
450MG/VIAL **Federal R...
PARAPLATIN
USA
19880
1989-03-03
DISCN
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US
PHARMACOMPASS
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your Marketing & Sales content
URL Supplier Web Content
INJECTABLE;INTRAVENOUS
50MG/5ML (10MG/ML) **F...
PARAPLATIN
USA
20452
2003-07-14
DISCN
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US
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your Marketing & Sales content
URL Supplier Web Content
INJECTABLE;INTRAVENOUS
150MG/15ML (10MG/ML) *...
PARAPLATIN
USA
20452
2003-07-14
DISCN
ASK
US
PHARMACOMPASS
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your Marketing & Sales content
URL Supplier Web Content
INJECTABLE;INTRAVENOUS
450MG/45ML (10MG/ML) *...
PARAPLATIN
USA
20452
2003-07-14
DISCN
ASK
US
PHARMACOMPASS
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your Marketing & Sales content
URL Supplier Web Content
INJECTABLE;INTRAVENOUS
600MG/60ML (10MG/ML) *...
PARAPLATIN
USA
20452
2004-01-15
DISCN
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URL Supplier Web Content
TABLET;ORAL
500MG **Federal Regist...
CEFZIL
USA
50664
1991-12-23
DISCN
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URL Supplier Web Content
FOR SUSPENSION;ORAL
125MG/5ML **Federal Re...
CEFZIL
USA
50665
1991-12-23
DISCN
ASK
US
PHARMACOMPASS
Upload
your Marketing & Sales content
URL Supplier Web Content
FOR SUSPENSION;ORAL
250MG/5ML **Federal Re...
CEFZIL
USA
50665
1991-12-23
DISCN
ASK
US
PHARMACOMPASS
Upload
your Marketing & Sales content
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