DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
DEPAKOTE ER
FDA Application No:
(NDA) 021168
Active Ingredient(s):
DIVALPROEX SODIUM
Company:
ABBOTT
Original Approval or Tentative Approval Date:
August 4, 2000
Chemical Type:
3 New dosage form
Review Classification:
S Standard review drug
There are no Therapeutic Equivalents
Label Information
Approval History, Letters, Reviews and Related Documents
You can see the products in the same application. The table can be sorted by clicking the header columns.
Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
DEPAKOTE ER
DIVALPROEX SODIUM
EQ 500MG VALPROIC ACID
TABLET, EXTENDED RELEASE; ORAL
Prescription
Yes
None
DEPAKOTE ER
DIVALPROEX SODIUM
EQ 250MG VALPROIC ACID
TABLET, EXTENDED RELEASE; ORAL
Prescription
No
None
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