"65841-738-05" National Drug Code (NDC)

Pramipexole Dihydrochloride 500 TABLET in 1 BOTTLE (65841-738-05)
(Zydus Lifesciences Limited)

NDC Code65841-738-05
Package Description500 TABLET in 1 BOTTLE (65841-738-05)
Product NDC65841-738
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePramipexole Dihydrochloride
Non-Proprietary NamePramipexole Dihydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20100710
Marketing Category NameANDA
Application NumberANDA078920
ManufacturerZydus Lifesciences Limited
Substance NamePRAMIPEXOLE DIHYDROCHLORIDE
Strength1.5
Strength Unitmg/1
Pharmacy ClassesDopamine Agonists [MoA], Nonergot Dopamine Agonist [EPC]

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