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"0781-5786-31" National Drug Code (NDC)
Ropinirole 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0781-5786-31)
(Sandoz Inc)
NDC Code
0781-5786-31
Package Description
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0781-5786-31)
Product NDC
0781-5786
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
20120901
Marketing Category Name
ANDA
Application Number
ANDA201047
Manufacturer
Sandoz Inc
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/0781-5786-31