Product Details for ANDA 076235
CARBOPLATIN (CARBOPLATIN)
50MG/VIAL
Marketing Status: Discontinued
150MG/VIAL
Marketing Status: Discontinued
450MG/VIAL
Marketing Status: Discontinued
50MG/VIAL
Marketing Status: Discontinued
Active Ingredient: CARBOPLATIN
Proprietary Name: CARBOPLATIN
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 50MG/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076235
Product Number: 001
Approval Date: Oct 14, 2004
Applicant Holder Full Name: FRESENIUS KABI USA LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
CARBOPLATIN (CARBOPLATIN)
Proprietary Name: CARBOPLATIN
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 50MG/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076235
Product Number: 001
Approval Date: Oct 14, 2004
Applicant Holder Full Name: FRESENIUS KABI USA LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
150MG/VIAL
Marketing Status: Discontinued
Active Ingredient: CARBOPLATIN
Proprietary Name: CARBOPLATIN
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 150MG/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076235
Product Number: 002
Approval Date: Oct 14, 2004
Applicant Holder Full Name: FRESENIUS KABI USA LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
CARBOPLATIN (CARBOPLATIN)
Proprietary Name: CARBOPLATIN
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 150MG/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076235
Product Number: 002
Approval Date: Oct 14, 2004
Applicant Holder Full Name: FRESENIUS KABI USA LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
450MG/VIAL
Marketing Status: Discontinued
Active Ingredient: CARBOPLATIN
Proprietary Name: CARBOPLATIN
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 450MG/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076235
Product Number: 003
Approval Date: Oct 14, 2004
Applicant Holder Full Name: FRESENIUS KABI USA LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: CARBOPLATIN
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 450MG/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076235
Product Number: 003
Approval Date: Oct 14, 2004
Applicant Holder Full Name: FRESENIUS KABI USA LLC
Marketing Status: Discontinued
Patent and Exclusivity Information