"57237-185-99" National Drug Code (NDC)

Pramipexole Dihydrochloride 1000 TABLET in 1 BOTTLE (57237-185-99)
(Rising Pharma Holdings, Inc.)

NDC Code57237-185-99
Package Description1000 TABLET in 1 BOTTLE (57237-185-99)
Product NDC57237-185
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePramipexole Dihydrochloride
Non-Proprietary NamePramipexole Dihydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20121026
Marketing Category NameANDA
Application NumberANDA202633
ManufacturerRising Pharma Holdings, Inc.
Substance NamePRAMIPEXOLE DIHYDROCHLORIDE
Strength1.5
Strength Unitmg/1
Pharmacy ClassesDopamine Agonists [MoA], Nonergot Dopamine Agonist [EPC]

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