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"49884-197-01" National Drug Code (NDC)

Oxycodone Hydrochloride 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (49884-197-01)
(Par Pharmaceutical, Inc.)

NDC Code49884-197-01
Package Description100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (49884-197-01)
Product NDC49884-197
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOxycodone Hydrochloride
Non-Proprietary NameOxycodone Hydrochloride
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20100808
End Marketing Date20201231
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA022272
ManufacturerPar Pharmaceutical, Inc.
Substance NameOXYCODONE HYDROCHLORIDE
Strength80
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/49884-197-01





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