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"16714-922-01" National Drug Code (NDC)

Pramipexole Dihydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-922-01)
(NorthStar RxLLC)

NDC Code16714-922-01
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-922-01)
Product NDC16714-922
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePramipexole Dihydrochloride
Non-Proprietary NamePramipexole Dihydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20190306
Marketing Category NameANDA
Application NumberANDA206156
ManufacturerNorthStar RxLLC
Substance NamePRAMIPEXOLE DIHYDROCHLORIDE
Strength4.5
Strength Unitmg/1
Pharmacy ClassesDopamine Agonists [MoA], Nonergot Dopamine Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/16714-922-01





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