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"72189-222-30" National Drug Code (NDC)
Ropinirole 30 TABLET, FILM COATED in 1 BOTTLE (72189-222-30)
(DIRECT RX)
NDC Code
72189-222-30
Package Description
30 TABLET, FILM COATED in 1 BOTTLE (72189-222-30)
Product NDC
72189-222
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ropinirole
Non-Proprietary Name
Ropinirole
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20210520
Marketing Category Name
ANDA
Application Number
ANDA204022
Manufacturer
DIRECT RX
Substance Name
ROPINIROLE HYDROCHLORIDE
Strength
1
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/72189-222-30