"0093-5733-01" National Drug Code (NDC)

Oxycodone Hydrochloride 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-5733-01)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-5733-01
Package Description100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-5733-01)
Product NDC0093-5733
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOxycodone Hydrochloride
Non-Proprietary NameOxycodone Hydrochloride
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20151014
End Marketing Date20250131
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA022272
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameOXYCODONE HYDROCHLORIDE
Strength40
Strength Unitmg/1
Pharmacy ClassesFull Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA ScheduleCII

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