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"70518-0211-0" National Drug Code (NDC)
Cyclobenzaprine Hydrochloride 20 TABLET in 1 BOTTLE, PLASTIC (70518-0211-0)
(REMEDYREPACK INC.)
NDC Code
70518-0211-0
Package Description
20 TABLET in 1 BOTTLE, PLASTIC (70518-0211-0)
Product NDC
70518-0211
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Cyclobenzaprine Hydrochloride
Non-Proprietary Name
Cyclobenzaprine Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20170209
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/70518-0211-0