"72189-222-30" National Drug Code (NDC)

Ropinirole 30 TABLET, FILM COATED in 1 BOTTLE (72189-222-30)
(DIRECT RX)

NDC Code72189-222-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (72189-222-30)
Product NDC72189-222
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRopinirole
Non-Proprietary NameRopinirole
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20210520
Marketing Category NameANDA
Application NumberANDA204022
ManufacturerDIRECT RX
Substance NameROPINIROLE HYDROCHLORIDE
Strength1
Strength Unitmg/1
Pharmacy ClassesDopamine Agonists [MoA], Nonergot Dopamine Agonist [EPC]

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