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"61919-261-15" National Drug Code (NDC)

Cyclobenzaprine Hydrochloride 15 TABLET, FILM COATED in 1 BOTTLE (61919-261-15)
(Direct_Rx)

NDC Code61919-261-15
Package Description15 TABLET, FILM COATED in 1 BOTTLE (61919-261-15)
Product NDC61919-261
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCyclobenzaprine Hydrochloride
Non-Proprietary NameCyclobenzaprine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190816
Marketing Category NameANDA
Application NumberANDA078722
ManufacturerDirect_Rx
Substance NameCYCLOBENZAPRINE HYDROCHLORIDE
Strength7.5
Strength Unitmg/1
Pharmacy ClassesCentrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-261-15





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