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"70518-2439-1" National Drug Code (NDC)

Ropinirole 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2439-1)
(REMEDYREPACK INC.)

NDC Code70518-2439-1
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2439-1)
Product NDC70518-2439
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRopinirole
Non-Proprietary NameRopinirole
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20191120
Marketing Category NameANDA
Application NumberANDA204022
ManufacturerREMEDYREPACK INC.
Substance NameROPINIROLE HYDROCHLORIDE
Strength.5
Strength Unitmg/1
Pharmacy ClassesDopamine Agonists [MoA], Nonergot Dopamine Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-2439-1





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