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"65841-717-10" National Drug Code (NDC)

Ropinirole Hydrochloride 1000 TABLET, FILM COATED in 1 BOTTLE (65841-717-10)
(Zydus Lifesciences Limited)

NDC Code65841-717-10
Package Description1000 TABLET, FILM COATED in 1 BOTTLE (65841-717-10)
Product NDC65841-717
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRopinirole Hydrochloride
Non-Proprietary NameRopinirole Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20090923
Marketing Category NameANDA
Application NumberANDA090411
ManufacturerZydus Lifesciences Limited
Substance NameROPINIROLE HYDROCHLORIDE
Strength4
Strength Unitmg/1
Pharmacy ClassesDopamine Agonists [MoA], Nonergot Dopamine Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/65841-717-10





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