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"70518-3159-1" National Drug Code (NDC)
Cyclobenzaprine Hydrochloride 5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3159-1)
(REMEDYREPACK INC.)
NDC Code
70518-3159-1
Package Description
5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3159-1)
Product NDC
70518-3159
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Cyclobenzaprine Hydrochloride
Non-Proprietary Name
Cyclobenzaprine
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20210715
Marketing Category Name
ANDA
Application Number
ANDA090478
Manufacturer
REMEDYREPACK 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/70518-3159-1