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"42291-535-90" National Drug Code (NDC)

Pramipexole 90 TABLET in 1 BOTTLE (42291-535-90)
(AvKARE, Inc.)

NDC Code42291-535-90
Package Description90 TABLET in 1 BOTTLE (42291-535-90)
Product NDC42291-535
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePramipexole
Non-Proprietary NamePramipexole
Dosage FormTABLET
UsageORAL
Start Marketing Date20160727
End Marketing Date20180702
Marketing Category NameANDA
Application NumberANDA203855
ManufacturerAvKARE, Inc.
Substance NamePRAMIPEXOLE DIHYDROCHLORIDE
Strength.25
Strength Unitmg/1
Pharmacy ClassesDopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/42291-535-90





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