"31722-909-05" National Drug Code (NDC)

Pramipexole 500 TABLET in 1 BOTTLE (31722-909-05)
(Camber Pharmaceuticals, Inc.)

NDC Code31722-909-05
Package Description500 TABLET in 1 BOTTLE (31722-909-05)
Product NDC31722-909
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePramipexole
Non-Proprietary NamePramipexole
Dosage FormTABLET
UsageORAL
Start Marketing Date20150801
Marketing Category NameANDA
Application NumberANDA203855
ManufacturerCamber Pharmaceuticals, Inc.
Substance NamePRAMIPEXOLE DIHYDROCHLORIDE
Strength.75
Strength Unitmg/1
Pharmacy ClassesDopamine Agonists [MoA], Nonergot Dopamine Agonist [EPC]

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