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"57664-223-88" National Drug Code (NDC)

Oxycodone Hydrochloride 100 TABLET in 1 BOTTLE (57664-223-88)
(Sun Pharmaceutical Industries, Inc.)

NDC Code57664-223-88
Package Description100 TABLET in 1 BOTTLE (57664-223-88)
Product NDC57664-223
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOxycodone Hydrochloride
Non-Proprietary NameOxycodone Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20090512
Marketing Category NameANDA
Application NumberANDA090659
ManufacturerSun Pharmaceutical Industries, Inc.
Substance NameOXYCODONE HYDROCHLORIDE
Strength5
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/57664-223-88





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