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"52959-042-21" National Drug Code (NDC)
Cyclobenzaprine Hydrochloride 21 TABLET, FILM COATED in 1 CONTAINER (52959-042-21)
(H. J Harkins Company Inc)
NDC Code
52959-042-21
Package Description
21 TABLET, FILM COATED in 1 CONTAINER (52959-042-21)
Product NDC
52959-042
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
20170103
Marketing Category Name
ANDA
Application Number
ANDA077797
Manufacturer
H. J Harkins Company Inc
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/52959-042-21