"50228-129-10" National Drug Code (NDC)

Pramipexole Dihydrochloride 1000 TABLET in 1 BOTTLE (50228-129-10)
(ScieGen Pharmaceuticals Inc)

NDC Code50228-129-10
Package Description1000 TABLET in 1 BOTTLE (50228-129-10)
Product NDC50228-129
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePramipexole Dihydrochloride
Non-Proprietary NamePramipexole Dihydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20141029
Marketing Category NameANDA
Application NumberANDA203855
ManufacturerScieGen Pharmaceuticals Inc
Substance NamePRAMIPEXOLE DIHYDROCHLORIDE
Strength.75
Strength Unitmg/1
Pharmacy ClassesDopamine Agonists [MoA], Nonergot Dopamine Agonist [EPC]

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