01 3PRINSTON INC
01 3TABLET, DELAYED RELEASE;ORAL
01 3RX
01 3DIVALPROEX SODIUM
01 3No
RLD : No
TE Code : AB
Dosage Form : TABLET, DELAYED RELEASE; ORAL
Proprietary Name : DIVALPROEX SODIUM
Dosage Strength : EQ 500MG VALPROIC ACID
Approval Date : 2009-11-30
Application Number : 90210
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET, DELAYED RELEASE; ORAL
Proprietary Name : DIVALPROEX SODIUM
Dosage Strength : EQ 125MG VALPROIC ACID
Approval Date : 2009-11-30
Application Number : 90210
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET, DELAYED RELEASE; ORAL
Proprietary Name : DIVALPROEX SODIUM
Dosage Strength : EQ 250MG VALPROIC ACID
Approval Date : 2009-11-30
Application Number : 90210
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
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