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"67046-137-21" National Drug Code (NDC)
Divalproex Sodium 21 TABLET, DELAYED RELEASE in 1 BLISTER PACK (67046-137-21)
(Contract Pharmacy Services-PA)
NDC Code
67046-137-21
Package Description
21 TABLET, DELAYED RELEASE in 1 BLISTER PACK (67046-137-21)
Product NDC
67046-137
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
20170925
Marketing Category Name
ANDA
Application Number
ANDA077100
Manufacturer
Contract Pharmacy Services-PA
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/67046-137-21