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"72189-080-21" National Drug Code (NDC)

Cyclobenzaprine Hydrochloride 21 TABLET, FILM COATED in 1 BOTTLE (72189-080-21)
(DIRECT RX)

NDC Code72189-080-21
Package Description21 TABLET, FILM COATED in 1 BOTTLE (72189-080-21)
Product NDC72189-080
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCyclobenzaprine Hydrochloride
Non-Proprietary NameCyclobenzaprine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20200513
Marketing Category NameANDA
Application NumberANDA208170
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/72189-080-21





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