"0093-5721-56" National Drug Code (NDC)

Buprenorphine And Naloxone 30 TABLET in 1 BOTTLE (0093-5721-56)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-5721-56
Package Description30 TABLET in 1 BOTTLE (0093-5721-56)
Product NDC0093-5721
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBuprenorphine And Naloxone
Non-Proprietary NameBuprenorphine And Naloxone
Dosage FormTABLET
UsageSUBLINGUAL
Start Marketing Date20141210
End Marketing Date20181031
Marketing Category NameANDA
Application NumberANDA091149
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameBUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE
Strength8; 2
Strength Unitmg/1; mg/1
Pharmacy ClassesPartial Opioid Agonist [EPC],Partial Opioid Agonists [MoA],Opioid Antagonist [EPC],Opioid Antagonists [MoA]
DEA ScheduleCIII

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