"61919-821-90" National Drug Code (NDC)

Oxycodone Hydrochloride 90 TABLET in 1 BOTTLE (61919-821-90)
(Direct_Rx)

NDC Code61919-821-90
Package Description90 TABLET in 1 BOTTLE (61919-821-90)
Product NDC61919-821
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOxycodone Hydrochloride
Non-Proprietary NameOxycodone Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20190708
Marketing Category NameANDA
Application NumberANDA203638
ManufacturerDirect_Rx
Substance NameOXYCODONE HYDROCHLORIDE
Strength5
Strength Unitmg/1
Pharmacy ClassesFull Opioid Agonists [MoA],Opioid Agonist [EPC]
DEA ScheduleCII

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