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"67296-1376-2" National Drug Code (NDC)

Oxycodone Hydrochloride 20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67296-1376-2)
(RedPharm Drug, Inc.)

NDC Code67296-1376-2
Package Description20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67296-1376-2)
Product NDC67296-1376
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOxycodone Hydrochloride
Non-Proprietary NameOxycodone Hydrochloride
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20160222
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA022272
ManufacturerRedPharm Drug, Inc.
Substance NameOXYCODONE HYDROCHLORIDE
Strength10
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/67296-1376-2





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