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"70518-0082-0" National Drug Code (NDC)
Cyclobenzaprine Hydrochloride 21 TABLET, FILM COATED in 1 BLISTER PACK (70518-0082-0)
(REMEDYREPACK INC.)
NDC Code
70518-0082-0
Package Description
21 TABLET, FILM COATED in 1 BLISTER PACK (70518-0082-0)
Product NDC
70518-0082
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Cyclobenzaprine Hydrochloride
Non-Proprietary Name
Cyclobenzaprine
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20161223
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/70518-0082-0