"70518-1723-0" National Drug Code (NDC)

Methocarbamol 30 TABLET, COATED in 1 BLISTER PACK (70518-1723-0)
(REMEDYREPACK INC.)

NDC Code70518-1723-0
Package Description30 TABLET, COATED in 1 BLISTER PACK (70518-1723-0)
Product NDC70518-1723
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMethocarbamol
Non-Proprietary NameMethocarbamol Tablets
Dosage FormTABLET, COATED
UsageORAL
Start Marketing Date20181210
Marketing Category NameANDA
Application NumberANDA209312
ManufacturerREMEDYREPACK INC.
Substance NameMETHOCARBAMOL
Strength500
Strength Unitmg/1
Pharmacy ClassesCentrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

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