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"72022-583-05" National Drug Code (NDC)

Oxycodone And Acetaminophen 500 TABLET in 1 BOTTLE (72022-583-05)
(Halo Pharmaceutical Inc)

NDC Code72022-583-05
Package Description500 TABLET in 1 BOTTLE (72022-583-05)
Product NDC72022-583
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOxycodone And Acetaminophen
Non-Proprietary NameOxycodone And Acetaminophen
Dosage FormTABLET
UsageORAL
Start Marketing Date20200215
Marketing Category NameANDA
Application NumberANDA207834
ManufacturerHalo Pharmaceutical Inc
Substance NameOXYCODONE HYDROCHLORIDE; ACETAMINOPHEN
Strength7.5; 325
Strength Unitmg/1; mg/1
Pharmacy ClassesFull Opioid Agonists [MoA],Opioid Agonist [EPC]
DEA ScheduleCII

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/72022-583-05





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