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"13811-642-10" National Drug Code (NDC)
Ropinirole 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (13811-642-10)
(Trigen Laboratories, LLC)
NDC Code
13811-642-10
Package Description
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (13811-642-10)
Product NDC
13811-642
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ropinirole
Non-Proprietary Name
Ropinirole
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20130314
End Marketing Date
20210228
Marketing Category Name
ANDA
Application Number
ANDA202786
Manufacturer
Trigen Laboratories, LLC
Substance Name
ROPINIROLE HYDROCHLORIDE
Strength
8
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/13811-642-10