"70518-0652-2" National Drug Code (NDC)

Buprenorphine Hydrochloride Sublingual 30 TABLET in 1 BOTTLE, PLASTIC (70518-0652-2)
(REMEDYREPACK INC.)

NDC Code70518-0652-2
Package Description30 TABLET in 1 BOTTLE, PLASTIC (70518-0652-2)
Product NDC70518-0652
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBuprenorphine Hydrochloride Sublingual
Non-Proprietary NameBuprenorphine Hydrochloride Sublingual
Dosage FormTABLET
UsageSUBLINGUAL
Start Marketing Date20170731
Marketing Category NameANDA
Application NumberANDA201066
ManufacturerREMEDYREPACK INC.
Substance NameBUPRENORPHINE HYDROCHLORIDE
Strength2
Strength Unitmg/1
Pharmacy ClassesPartial Opioid Agonists [MoA],Partial Opioid Agonist [EPC]
DEA ScheduleCIII

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