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"62037-667-01" National Drug Code (NDC)

Divalproex Sodium 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (62037-667-01)
(Watson Pharma, Inc.)

NDC Code62037-667-01
Package Description100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (62037-667-01)
Product NDC62037-667
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDivalproex Sodium
Non-Proprietary NameDivalproex Sodium
Dosage FormTABLET, DELAYED RELEASE
UsageORAL
Start Marketing Date20110225
Marketing Category NameANDA
Application NumberANDA079080
ManufacturerWatson Pharma, Inc.
Substance NameDIVALPROEX SODIUM
Strength500
Strength Unitmg/1
Pharmacy ClassesAnti-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/62037-667-01





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