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"0781-5032-64" National Drug Code (NDC)
Cyclobenzaprine Hydrochloride 10 TABLET, FILM COATED in 1 BLISTER PACK (0781-5032-64)
(Sandoz Inc)
NDC Code
0781-5032-64
Package Description
10 TABLET, FILM COATED in 1 BLISTER PACK (0781-5032-64)
Product NDC
0781-5032
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
20060206
Marketing Category Name
ANDA
Application Number
ANDA072854
Manufacturer
Sandoz 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/0781-5032-64