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Pramipexole Dihydrochloride - 16714-589-01 - (Pramipexole Dihydrochloride)

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Drug Information of Pramipexole Dihydrochloride

Product NDC: 16714-589
Proprietary Name: Pramipexole Dihydrochloride
Non Proprietary Name: Pramipexole Dihydrochloride
Active Ingredient(s): .75    mg/1 & nbsp;   Pramipexole Dihydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Pramipexole Dihydrochloride

Product NDC: 16714-589
Labeler Name: Northstar Rx LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091254
Marketing Category: ANDA
Start Marketing Date: 20101130

Package Information of Pramipexole Dihydrochloride

Package NDC: 16714-589-01
Package Description: 90 TABLET in 1 BOTTLE (16714-589-01)

NDC Information of Pramipexole Dihydrochloride

NDC Code 16714-589-01
Proprietary Name Pramipexole Dihydrochloride
Package Description 90 TABLET in 1 BOTTLE (16714-589-01)
Product NDC 16714-589
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pramipexole Dihydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101130
Marketing Category Name ANDA
Labeler Name Northstar Rx LLC
Substance Name PRAMIPEXOLE DIHYDROCHLORIDE
Strength Number .75
Strength Unit mg/1
Pharmaceutical Classes Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC]

Complete Information of Pramipexole Dihydrochloride


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