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Pramipexole Dihydrochloride - 0781-5281-31 - (Pramipexole Dihydrochloride)

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Drug Information of Pramipexole Dihydrochloride

Product NDC: 0781-5281
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: 0781-5281
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090190
Marketing Category: ANDA
Start Marketing Date: 20101008

Package Information of Pramipexole Dihydrochloride

Package NDC: 0781-5281-31
Package Description: 30 TABLET in 1 BOTTLE (0781-5281-31)

NDC Information of Pramipexole Dihydrochloride

NDC Code 0781-5281-31
Proprietary Name Pramipexole Dihydrochloride
Package Description 30 TABLET in 1 BOTTLE (0781-5281-31)
Product NDC 0781-5281
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pramipexole Dihydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101008
Marketing Category Name ANDA
Labeler Name Sandoz Inc
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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