Mirapex - 21695-867-90 - (pramipexole dihydrochloride)

Alphabetical Index


Drug Information of Mirapex

Product NDC: 21695-867
Proprietary Name: Mirapex
Non Proprietary Name: pramipexole dihydrochloride
Active Ingredient(s): .5    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: 21695-867
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020667
Marketing Category: NDA
Start Marketing Date: 20040101

Package Information of Mirapex

Package NDC: 21695-867-90
Package Description: 90 TABLET in 1 BOTTLE (21695-867-90)

NDC Information of Mirapex

NDC Code 21695-867-90
Proprietary Name Mirapex
Package Description 90 TABLET in 1 BOTTLE (21695-867-90)
Product NDC 21695-867
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 Rebel Distributors Corp
Substance Name PRAMIPEXOLE DIHYDROCHLORIDE
Strength Number .5
Strength Unit mg/1
Pharmaceutical Classes Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC]

Complete Information of Mirapex


General Information