"70518-3474-7" National Drug Code (NDC)

Cyclobenzaprine Hydrochloride 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3474-7)
(REMEDYREPACK INC.)

NDC Code70518-3474-7
Package Description20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3474-7)
Product NDC70518-3474
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCyclobenzaprine Hydrochloride
Non-Proprietary NameCyclobenzaprine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20220809
Marketing Category NameANDA
Application NumberANDA078643
ManufacturerREMEDYREPACK INC.
Substance NameCYCLOBENZAPRINE HYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesCentrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]

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