CordenPharma
FDA Approved Drugs
CordenPharma
FDA Approved Drugs Database
FDA approved drug product records including application numbers, product numbers, drug names, active ingredients, dosage forms, strengths, approval dates and regulatory status.
- Total Records 12
- Latest Approval Date Jan 15, 2004
- Data Source FDA
- First Approval Date Nov 10, 1983
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CordenPharma
Otto-Hahn-Strasse 68723 Plankstadt
Germany
www.cordenpharma.com/ sales@cordenpharma.com View on MapFDA Approved Drug Records ( 12 records )
Drug Name
CEFZIL
Product Number
1
Dosage Form
-
Strength
250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1991-12-23
Active Ingredient
CEFPROZIL
Application Number
50664
Product Number
1
Dosage Form
-
Strength
250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1991-12-23
Regulatory Status
Discontinued
Drug Name
CEFZIL
Product Number
2
Dosage Form
-
Strength
500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1991-12-23
Active Ingredient
CEFPROZIL
Application Number
50664
Product Number
2
Dosage Form
-
Strength
500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1991-12-23
Regulatory Status
Discontinued
Drug Name
CEFZIL
Product Number
1
Dosage Form
-
Strength
125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1991-12-23
Active Ingredient
CEFPROZIL
Application Number
50665
Product Number
1
Dosage Form
-
Strength
125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1991-12-23
Regulatory Status
Discontinued
Drug Name
CEFZIL
Product Number
2
Dosage Form
-
Strength
250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1991-12-23
Active Ingredient
CEFPROZIL
Application Number
50665
Product Number
2
Dosage Form
-
Strength
250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1991-12-23
Regulatory Status
Discontinued
Drug Name
PARAPLATIN
Product Number
1
Dosage Form
-
Strength
50MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1989-03-03
Active Ingredient
CARBOPLATIN
Application Number
19880
Product Number
1
Dosage Form
-
Strength
50MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1989-03-03
Regulatory Status
Discontinued
Drug Name
PARAPLATIN
Product Number
2
Dosage Form
-
Strength
150MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1989-03-03
Active Ingredient
CARBOPLATIN
Application Number
19880
Product Number
2
Dosage Form
-
Strength
150MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1989-03-03
Regulatory Status
Discontinued
Drug Name
PARAPLATIN
Product Number
3
Dosage Form
-
Strength
450MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1989-03-03
Active Ingredient
CARBOPLATIN
Application Number
19880
Product Number
3
Dosage Form
-
Strength
450MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1989-03-03
Regulatory Status
Discontinued
Drug Name
PARAPLATIN
Product Number
1
Dosage Form
-
Strength
50MG/5ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2003-07-14
Active Ingredient
CARBOPLATIN
Application Number
20452
Product Number
1
Dosage Form
-
Strength
50MG/5ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2003-07-14
Regulatory Status
Discontinued
Drug Name
PARAPLATIN
Product Number
2
Dosage Form
-
Strength
150MG/15ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2003-07-14
Active Ingredient
CARBOPLATIN
Application Number
20452
Product Number
2
Dosage Form
-
Strength
150MG/15ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2003-07-14
Regulatory Status
Discontinued
Drug Name
PARAPLATIN
Product Number
3
Dosage Form
-
Strength
450MG/45ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2003-07-14
Active Ingredient
CARBOPLATIN
Application Number
20452
Product Number
3
Dosage Form
-
Strength
450MG/45ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2003-07-14
Regulatory Status
Discontinued
Drug Name
PARAPLATIN
Product Number
4
Dosage Form
-
Strength
600MG/60ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2004-01-15
Active Ingredient
CARBOPLATIN
Application Number
20452
Product Number
4
Dosage Form
-
Strength
600MG/60ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2004-01-15
Regulatory Status
Discontinued
Drug Name
VEPESID
Product Number
1
Dosage Form
-
Strength
20MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1983-11-10
Active Ingredient
ETOPOSIDE
Application Number
18768
Product Number
1
Dosage Form
-
Strength
20MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1983-11-10
Regulatory Status
Discontinued
Drug Status Breakdown
12 total- Discontinued
Official Source
FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.
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Drug Name
CEFZIL
Application Number
50664
Product Number
1
Active Ingredient
CEFPROZIL
Dosage Form
-
Strength
250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
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