Mirapex - 55154-0409-0 - (pramipexole dihydrochloride)

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Drug Information of Mirapex

Product NDC: 55154-0409
Proprietary Name: Mirapex
Non Proprietary Name: pramipexole dihydrochloride
Active Ingredient(s): .25    mg/1 & nbsp;   pramipexole dihydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Mirapex

Product NDC: 55154-0409
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020667
Marketing Category: NDA
Start Marketing Date: 20040101

Package Information of Mirapex

Package NDC: 55154-0409-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-0409-0) > 1 TABLET in 1 BLISTER PACK

NDC Information of Mirapex

NDC Code 55154-0409-0
Proprietary Name Mirapex
Package Description 10 BLISTER PACK in 1 BAG (55154-0409-0) > 1 TABLET in 1 BLISTER PACK
Product NDC 55154-0409
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name pramipexole dihydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040101
Marketing Category Name NDA
Labeler Name Cardinal Health
Substance Name PRAMIPEXOLE DIHYDROCHLORIDE
Strength Number .25
Strength Unit mg/1
Pharmaceutical Classes Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC]

Complete Information of Mirapex


General Information