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"72189-364-30" National Drug Code (NDC)
Ropinirole 30 TABLET, FILM COATED in 1 BOTTLE (72189-364-30)
(Direct_Rx)
NDC Code
72189-364-30
Package Description
30 TABLET, FILM COATED in 1 BOTTLE (72189-364-30)
Product NDC
72189-364
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ropinirole
Non-Proprietary Name
Ropinirole
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20220621
Marketing Category Name
ANDA
Application Number
ANDA204022
Manufacturer
Direct_Rx
Substance Name
ROPINIROLE HYDROCHLORIDE
Strength
.25
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/72189-364-30