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DepakoteDrug - Depakote The trade name of the product as shown on the labeling.
Dosage -
TABLET, DELAYED RELEASE; ORAL
Active Ingredient(s) -
Divalproex Sodium
Strength -
EQ 250MG VALPROIC ACID
Applicant -
ABBOTT
New Drug Application (NDA) Number -
018723
Product Number -
001
Therapeutic Equivalence (TE) Code -
Approval Date -
Mar 10, 1983
Reference Listed Drug (RLD) -
No
Type -
RX
Applicant Full Name -
Abbott Laboratories
Depakote
Disulfiram 250mg Tablet; Oral
Disulfiram 500mg Tablet; Oral Disulfiram 250mg Tablet; Oral Disulfiram 250mg Tablet; Oral Disulfiram 500mg Tablet; Oral Disulfiram 500mg Tablet; Oral Depakote Eq 125mg Valproic Acid Capsule, Delayed Rel Pellets; Oral Depakote Eq 125mg Valproic Acid Tablet, Delayed Release; Oral Depakote Eq 250mg Valproic Acid Tablet, Delayed Release; Oral Antabuse 500mg **federal Register Determination That Product Was Not Discontinued Or Withdrawn For Safety Or Efficacy Reasons** Tablet; Oral NewDrugInformation |