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Pramipexole Dihydrochloride - 42291-680-90 - (Pramipexole Dihydrochloride)

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Drug Information of Pramipexole Dihydrochloride

Product NDC: 42291-680
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: 42291-680
Labeler Name: AvKARE, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091450
Marketing Category: ANDA
Start Marketing Date: 20101008

Package Information of Pramipexole Dihydrochloride

Package NDC: 42291-680-90
Package Description: 90 TABLET in 1 BOTTLE (42291-680-90)

NDC Information of Pramipexole Dihydrochloride

NDC Code 42291-680-90
Proprietary Name Pramipexole Dihydrochloride
Package Description 90 TABLET in 1 BOTTLE (42291-680-90)
Product NDC 42291-680
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 AvKARE, Inc.
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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