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"69452-435-30" National Drug Code (NDC)

Divalproex Sodium 500 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-435-30)
(Bionpharma Inc.)

NDC Code69452-435-30
Package Description500 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-435-30)
Product NDC69452-435
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDivalproex Sodium
Non-Proprietary NameDivalproex Sodium
Dosage FormTABLET, DELAYED RELEASE
UsageORAL
Start Marketing Date20240626
Marketing Category NameANDA
Application NumberANDA078853
ManufacturerBionpharma 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/69452-435-30





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