"64679-771-03" National Drug Code (NDC)

Ropinirole Hydrochloride 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64679-771-03)
(Wockhardt USA LLC.)

NDC Code64679-771-03
Package Description500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64679-771-03)
Product NDC64679-771
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRopinirole Hydrochloride
Non-Proprietary NameRopinirole Hydrochloride
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20120815
Marketing Category NameANDA
Application NumberANDA091395
ManufacturerWockhardt USA LLC.
Substance NameROPINIROLE HYDROCHLORIDE
Strength2
Strength Unitmg/1
Pharmacy ClassesDopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC]

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