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"71335-1626-3" National Drug Code (NDC)
Ropinirole Hydrochloride 90 TABLET, FILM COATED in 1 BOTTLE (71335-1626-3)
(Bryant Ranch Prepack)
NDC Code
71335-1626-3
Package Description
90 TABLET, FILM COATED in 1 BOTTLE (71335-1626-3)
Product NDC
71335-1626
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ropinirole Hydrochloride
Non-Proprietary Name
Ropinirole Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20110920
Marketing Category Name
ANDA
Application Number
ANDA078110
Manufacturer
Bryant Ranch Prepack
Substance Name
ROPINIROLE HYDROCHLORIDE
Strength
2
Strength Unit
mg/1
Pharmacy Classes
Dopamine Agonists [MoA], Nonergot Dopamine Agonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-1626-3