"68084-305-01" National Drug Code (NDC)

Ropinirole Hydrochloride 10 BLISTER PACK in 1 CARTON (68084-305-01) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-305-11)
(American Health Packaging)

NDC Code68084-305-01
Package Description10 BLISTER PACK in 1 CARTON (68084-305-01) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-305-11)
Product NDC68084-305
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRopinirole Hydrochloride
Non-Proprietary NameRopinirole Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20130705
Marketing Category NameANDA
Application NumberANDA079050
ManufacturerAmerican Health Packaging
Substance NameROPINIROLE HYDROCHLORIDE
Strength.25
Strength Unitmg/1
Pharmacy ClassesDopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC]

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