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"61919-537-21" National Drug Code (NDC)

Cyclobenzaprine Hydrochloride 21 TABLET, FILM COATED in 1 BOTTLE (61919-537-21)
(Direct_Rx)

NDC Code61919-537-21
Package Description21 TABLET, FILM COATED in 1 BOTTLE (61919-537-21)
Product NDC61919-537
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCyclobenzaprine Hydrochloride
Non-Proprietary NameCyclobenzaprine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190823
Marketing Category NameANDA
Application NumberANDA077797
ManufacturerDirect_Rx
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/61919-537-21





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