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"68382-339-10" National Drug Code (NDC)

Ropinirole Hydrochloride 1000 TABLET, FILM COATED in 1 BOTTLE (68382-339-10)
(Zydus Pharmaceuticals (USA) Inc.)

NDC Code68382-339-10
Package Description1000 TABLET, FILM COATED in 1 BOTTLE (68382-339-10)
Product NDC68382-339
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 Pharmaceuticals (USA) 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/68382-339-10





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