"68382-134-16" National Drug Code (NDC)

Divalproex Sodium 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-134-16)
(Zydus Pharmaceuticals USA Inc.)

NDC Code68382-134-16
Package Description90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-134-16)
Product NDC68382-134
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDivalproex Sodium
Non-Proprietary NameDivalproex Sodium
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20130107
Marketing Category NameANDA
Application NumberANDA078239
ManufacturerZydus Pharmaceuticals USA 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/68382-134-16