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"70518-2209-0" National Drug Code (NDC)

Methocarbamol 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2209-0)
(REMEDYREPACK INC.)

NDC Code70518-2209-0
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2209-0)
Product NDC70518-2209
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMethocarbamol
Non-Proprietary NameMethocarbamol
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190711
Marketing Category NameANDA
Application NumberANDA208507
ManufacturerREMEDYREPACK INC.
Substance NameMETHOCARBAMOL
Strength750
Strength Unitmg/1
Pharmacy ClassesCentrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-2209-0





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