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"70518-0191-0" National Drug Code (NDC)
Cyclobenzaprine Hydrochloride 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0191-0)
(REMEDYREPACK INC.)
NDC Code
70518-0191-0
Package Description
30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0191-0)
Product NDC
70518-0191
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
20170202
Marketing Category Name
ANDA
Application Number
ANDA078048
Manufacturer
REMEDYREPACK INC.
Substance Name
CYCLOBENZAPRINE HYDROCHLORIDE
Strength
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/70518-0191-0