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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 075091

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CARBIDOPA AND LEVODOPA (CARBIDOPA; LEVODOPA)
25MG;100MG
Marketing Status: Prescription
Active Ingredient: CARBIDOPA; LEVODOPA
Proprietary Name: CARBIDOPA AND LEVODOPA
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 25MG;100MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A075091
Product Number: 002
Approval Date: Apr 21, 2000
Applicant Holder Full Name: MYLAN PHARMACEUTICALS INC
Marketing Status:  Prescription
Patent and Exclusivity Information
CARBIDOPA AND LEVODOPA (CARBIDOPA; LEVODOPA)
50MG;200MG
Marketing Status: Prescription
Active Ingredient: CARBIDOPA; LEVODOPA
Proprietary Name: CARBIDOPA AND LEVODOPA
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 50MG;200MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A075091
Product Number: 001
Approval Date: Sep 30, 1999
Applicant Holder Full Name: MYLAN PHARMACEUTICALS INC
Marketing Status:  Prescription
Patent and Exclusivity Information
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