Product Details for ANDA 090062
DIVALPROEX SODIUM (DIVALPROEX SODIUM)
EQ 125MG VALPROIC ACID
Marketing Status: Discontinued
EQ 250MG VALPROIC ACID
Marketing Status: Discontinued
EQ 500MG VALPROIC ACID
Marketing Status: Discontinued
EQ 125MG VALPROIC ACID
Marketing Status: Discontinued
Active Ingredient: DIVALPROEX SODIUM
Proprietary Name: DIVALPROEX SODIUM
Dosage Form; Route of Administration: TABLET, DELAYED RELEASE; ORAL
Strength: EQ 125MG VALPROIC ACID
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A090062
Product Number: 001
Approval Date: Mar 17, 2009
Applicant Holder Full Name: MYLAN PHARMACEUTICALS INC
Marketing Status: Discontinued
Patent and Exclusivity Information
DIVALPROEX SODIUM (DIVALPROEX SODIUM)
Proprietary Name: DIVALPROEX SODIUM
Dosage Form; Route of Administration: TABLET, DELAYED RELEASE; ORAL
Strength: EQ 125MG VALPROIC ACID
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A090062
Product Number: 001
Approval Date: Mar 17, 2009
Applicant Holder Full Name: MYLAN PHARMACEUTICALS INC
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 250MG VALPROIC ACID
Marketing Status: Discontinued
Active Ingredient: DIVALPROEX SODIUM
Proprietary Name: DIVALPROEX SODIUM
Dosage Form; Route of Administration: TABLET, DELAYED RELEASE; ORAL
Strength: EQ 250MG VALPROIC ACID
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A090062
Product Number: 002
Approval Date: Mar 17, 2009
Applicant Holder Full Name: MYLAN PHARMACEUTICALS INC
Marketing Status: Discontinued
Patent and Exclusivity Information
DIVALPROEX SODIUM (DIVALPROEX SODIUM)
Proprietary Name: DIVALPROEX SODIUM
Dosage Form; Route of Administration: TABLET, DELAYED RELEASE; ORAL
Strength: EQ 250MG VALPROIC ACID
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A090062
Product Number: 002
Approval Date: Mar 17, 2009
Applicant Holder Full Name: MYLAN PHARMACEUTICALS INC
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 500MG VALPROIC ACID
Marketing Status: Discontinued
Active Ingredient: DIVALPROEX SODIUM
Proprietary Name: DIVALPROEX SODIUM
Dosage Form; Route of Administration: TABLET, DELAYED RELEASE; ORAL
Strength: EQ 500MG VALPROIC ACID
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A090062
Product Number: 003
Approval Date: Mar 17, 2009
Applicant Holder Full Name: MYLAN PHARMACEUTICALS INC
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: DIVALPROEX SODIUM
Dosage Form; Route of Administration: TABLET, DELAYED RELEASE; ORAL
Strength: EQ 500MG VALPROIC ACID
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A090062
Product Number: 003
Approval Date: Mar 17, 2009
Applicant Holder Full Name: MYLAN PHARMACEUTICALS INC
Marketing Status: Discontinued
Patent and Exclusivity Information