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"0093-5286-01" National Drug Code (NDC)
Ropinirole Hydrochloride 100 TABLET, FILM COATED in 1 BOTTLE (0093-5286-01)
(Teva Pharmaceuticals USA Inc)
NDC Code
0093-5286-01
Package Description
100 TABLET, FILM COATED in 1 BOTTLE (0093-5286-01)
Product NDC
0093-5286
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
20080507
End Marketing Date
20140531
Marketing Category Name
ANDA
Application Number
ANDA077460
Manufacturer
Teva Pharmaceuticals USA Inc
Substance Name
ROPINIROLE HYDROCHLORIDE
Strength
3
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/0093-5286-01