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Pramipexole dihydrochloride - 33342-031-10 - (Pramipexole dihydrochloride)

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Drug Information of Pramipexole dihydrochloride

Product NDC: 33342-031
Proprietary Name: Pramipexole dihydrochloride
Non Proprietary Name: Pramipexole dihydrochloride
Active Ingredient(s): .125    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: 33342-031
Labeler Name: Macleods Pharmaceuticals Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202164
Marketing Category: ANDA
Start Marketing Date: 20120921

Package Information of Pramipexole dihydrochloride

Package NDC: 33342-031-10
Package Description: 90 TABLET in 1 BOTTLE (33342-031-10)

NDC Information of Pramipexole dihydrochloride

NDC Code 33342-031-10
Proprietary Name Pramipexole dihydrochloride
Package Description 90 TABLET in 1 BOTTLE (33342-031-10)
Product NDC 33342-031
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pramipexole dihydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120921
Marketing Category Name ANDA
Labeler Name Macleods Pharmaceuticals Limited
Substance Name PRAMIPEXOLE DIHYDROCHLORIDE
Strength Number .125
Strength Unit mg/1
Pharmaceutical Classes Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC]

Complete Information of Pramipexole dihydrochloride


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