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"53808-1027-1" National Drug Code (NDC)
Divalproex Sodium 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (53808-1027-1)
(State of Florida DOH Central Pharmacy)
NDC Code
53808-1027-1
Package Description
30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (53808-1027-1)
Product NDC
53808-1027
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Divalproex Sodium
Non-Proprietary Name
Divalproex Sodium
Dosage Form
TABLET, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20141101
Marketing Category Name
ANDA
Application Number
ANDA078182
Manufacturer
State of Florida DOH Central Pharmacy
Substance Name
DIVALPROEX SODIUM
Strength
250
Strength Unit
mg/1
Pharmacy Classes
Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/53808-1027-1