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"70518-0635-3" National Drug Code (NDC)

Cyclobenzaprine Hydrochloride 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0635-3)
(REMEDYREPACK INC.)

NDC Code70518-0635-3
Package Description15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0635-3)
Product NDC70518-0635
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCyclobenzaprine Hydrochloride
Non-Proprietary NameCyclobenzaprine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20170725
Marketing Category NameANDA
Application NumberANDA090478
ManufacturerREMEDYREPACK INC.
Substance NameCYCLOBENZAPRINE HYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesCentrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-0635-3





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