"70518-2691-0" National Drug Code (NDC)

Myambutol 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2691-0)
(REMEDYREPACK INC.)

NDC Code70518-2691-0
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2691-0)
Product NDC70518-2691
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMyambutol
Non-Proprietary NameEthambutol Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20200414
Marketing Category NameNDA
Application NumberNDA016320
ManufacturerREMEDYREPACK INC.
Substance NameETHAMBUTOL HYDROCHLORIDE
Strength400
Strength Unitmg/1
Pharmacy ClassesAntimycobacterial [EPC]

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