"70518-0669-0" National Drug Code (NDC)

Metoclopramide 30 TABLET in 1 BLISTER PACK (70518-0669-0)
(REMEDYREPACK INC.)

NDC Code70518-0669-0
Package Description30 TABLET in 1 BLISTER PACK (70518-0669-0)
Product NDC70518-0669
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMetoclopramide
Non-Proprietary NameMetoclopramide
Dosage FormTABLET
UsageORAL
Start Marketing Date20190814
Marketing Category NameANDA
Application NumberANDA070184
ManufacturerREMEDYREPACK INC.
Substance NameMETOCLOPRAMIDE HYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesDopamine D2 Antagonists [MoA], Dopamine-2 Receptor Antagonist [EPC]

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