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"61919-537-20" National Drug Code (NDC)
Cyclobenzaprine Hydrochloride 20 TABLET, FILM COATED in 1 BOTTLE (61919-537-20)
(Direct_Rx)
NDC Code
61919-537-20
Package Description
20 TABLET, FILM COATED in 1 BOTTLE (61919-537-20)
Product NDC
61919-537
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Cyclobenzaprine Hydrochloride
Non-Proprietary Name
Cyclobenzaprine Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20190813
Marketing Category Name
ANDA
Application Number
ANDA077797
Manufacturer
Direct_Rx
Substance Name
CYCLOBENZAPRINE HYDROCHLORIDE
Strength
10
Strength Unit
mg/1
Pharmacy Classes
Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-537-20