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"70518-2216-0" National Drug Code (NDC)

Buprenorphine Hydrochloride 30 TABLET in 1 BLISTER PACK (70518-2216-0)
(REMEDYREPACK INC.)

NDC Code70518-2216-0
Package Description30 TABLET in 1 BLISTER PACK (70518-2216-0)
Product NDC70518-2216
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBuprenorphine Hydrochloride
Non-Proprietary NameBuprenorphine Hydrochloride
Dosage FormTABLET
UsageSUBLINGUAL
Start Marketing Date20190715
End Marketing Date20250331
Marketing Category NameANDA
Application NumberANDA090622
ManufacturerREMEDYREPACK INC.
Substance NameBUPRENORPHINE HYDROCHLORIDE
Strength2
Strength Unitmg/1
Pharmacy ClassesPartial Opioid Agonist [EPC], Partial Opioid Agonists [MoA]
DEA ScheduleCIII

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-2216-0





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