Product Details for ANDA 077296
DIVALPROEX SODIUM (DIVALPROEX SODIUM)
EQ 125MG VALPROIC ACID
Marketing Status: Prescription
EQ 250MG VALPROIC ACID
Marketing Status: Prescription
EQ 500MG VALPROIC ACID
Marketing Status: Prescription
EQ 125MG VALPROIC ACID
Marketing Status: Prescription
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: AB
Application Number: A077296
Product Number: 001
Approval Date: Jul 31, 2008
Applicant Holder Full Name: CHARTWELL RX SCIENCES LLC
Marketing Status: Prescription
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: AB
Application Number: A077296
Product Number: 001
Approval Date: Jul 31, 2008
Applicant Holder Full Name: CHARTWELL RX SCIENCES LLC
Marketing Status: Prescription
Patent and Exclusivity Information
EQ 250MG VALPROIC ACID
Marketing Status: Prescription
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: AB
Application Number: A077296
Product Number: 002
Approval Date: Jul 31, 2008
Applicant Holder Full Name: CHARTWELL RX SCIENCES LLC
Marketing Status: Prescription
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: AB
Application Number: A077296
Product Number: 002
Approval Date: Jul 31, 2008
Applicant Holder Full Name: CHARTWELL RX SCIENCES LLC
Marketing Status: Prescription
Patent and Exclusivity Information
EQ 500MG VALPROIC ACID
Marketing Status: Prescription
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: AB
Application Number: A077296
Product Number: 003
Approval Date: Jul 31, 2008
Applicant Holder Full Name: CHARTWELL RX SCIENCES LLC
Marketing Status: Prescription
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: AB
Application Number: A077296
Product Number: 003
Approval Date: Jul 31, 2008
Applicant Holder Full Name: CHARTWELL RX SCIENCES LLC
Marketing Status: Prescription
Patent and Exclusivity Information