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"61919-681-72" National Drug Code (NDC)
Cyclobenzaprine Hci 72 TABLET, FILM COATED in 1 BOTTLE (61919-681-72)
(DIRECTRX)
NDC Code
61919-681-72
Package Description
72 TABLET, FILM COATED in 1 BOTTLE (61919-681-72)
Product NDC
61919-681
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Cyclobenzaprine Hci
Non-Proprietary Name
Cyclobenzaprine Hci
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20190402
Marketing Category Name
ANDA
Application Number
ANDA078722
Manufacturer
DIRECTRX
Substance Name
CYCLOBENZAPRINE HYDROCHLORIDE
Strength
7.5
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/61919-681-72