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"0781-5767-01" National Drug Code (NDC)

Oxycodone Hydrochloride 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0781-5767-01)
(Sandoz Inc)

NDC Code0781-5767-01
Package Description100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0781-5767-01)
Product NDC0781-5767
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOxycodone Hydrochloride
Non-Proprietary NameOxycodone Hydrochloride
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20141008
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA022272
ManufacturerSandoz Inc
Substance NameOXYCODONE HYDROCHLORIDE
Strength40
Strength Unitmg/1
Pharmacy ClassesFull Opioid Agonists [MoA],Opioid Agonist [EPC]
DEA ScheduleCII

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0781-5767-01





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