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"72789-354-01" National Drug Code (NDC)
Divalproex Sodium 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-354-01)
(PD-Rx Pharmaceuticals, Inc.)
NDC Code
72789-354-01
Package Description
100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-354-01)
Product NDC
72789-354
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
20080729
Marketing Category Name
ANDA
Application Number
ANDA078597
Manufacturer
PD-Rx Pharmaceuticals, Inc.
Substance Name
DIVALPROEX SODIUM
Strength
500
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/72789-354-01