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U.S. Department of Health and Human Services

Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Search results from the "OB_Rx" table for query on "018723."



Active Ingredient: DIVALPROEX SODIUM
Dosage Form;Route: TABLET, DELAYED RELEASE;ORAL
Proprietary Name: DEPAKOTE
Applicant: ABBVIE
Strength: EQ 250MG VALPROIC ACID
Application Number: N018723
Product Number: 001
Approval Date: Mar 10, 1983
Reference Listed Drug No
RX/OTC/DISCN: RX
TE Code: AB
Patent and Exclusivity Info for this product: View

Active Ingredient: DIVALPROEX SODIUM
Dosage Form;Route: TABLET, DELAYED RELEASE;ORAL
Proprietary Name: DEPAKOTE
Applicant: ABBVIE
Strength: EQ 500MG VALPROIC ACID
Application Number: N018723
Product Number: 002
Approval Date: Mar 10, 1983
Reference Listed Drug Yes
RX/OTC/DISCN: RX
TE Code: AB
Patent and Exclusivity Info for this product: View

Active Ingredient: DIVALPROEX SODIUM
Dosage Form;Route: TABLET, DELAYED RELEASE;ORAL
Proprietary Name: DEPAKOTE
Applicant: ABBVIE
Strength: EQ 125MG VALPROIC ACID
Application Number: N018723
Product Number: 003
Approval Date: Oct 26, 1984
Reference Listed Drug No
RX/OTC/DISCN: RX
TE Code: AB
Patent and Exclusivity Info for this product: View

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FDA/Center for Drug Evaluation and Research
Office of Generic Drugs
Division of Labeling and Program Support
Update Frequency:

Orange Book Data - Monthly
Generic Drug Product Information & Patent Information - Daily
Orange Book Data Updated Through July 2014
Patent and Generic Drug Product Data Last Updated August 29, 2014

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