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Pramipexole Dihydrochloride - 60951-937-92 - (Pramipexole Dihydrochloride Tablets)

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Drug Information of Pramipexole Dihydrochloride

Product NDC: 60951-937
Proprietary Name: Pramipexole Dihydrochloride
Non Proprietary Name: Pramipexole Dihydrochloride Tablets
Active Ingredient(s): 1.5    mg/1 & nbsp;   Pramipexole Dihydrochloride Tablets
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Pramipexole Dihydrochloride

Product NDC: 60951-937
Labeler Name: Endo Pharmaceuticals Inc. DBA Endo Generic Products
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078894
Marketing Category: ANDA
Start Marketing Date: 20101009

Package Information of Pramipexole Dihydrochloride

Package NDC: 60951-937-92
Package Description: 90 TABLET in 1 BOTTLE (60951-937-92)

NDC Information of Pramipexole Dihydrochloride

NDC Code 60951-937-92
Proprietary Name Pramipexole Dihydrochloride
Package Description 90 TABLET in 1 BOTTLE (60951-937-92)
Product NDC 60951-937
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pramipexole Dihydrochloride Tablets
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101009
Marketing Category Name ANDA
Labeler Name Endo Pharmaceuticals Inc. DBA Endo Generic Products
Substance Name PRAMIPEXOLE DIHYDROCHLORIDE
Strength Number 1.5
Strength Unit mg/1
Pharmaceutical Classes Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC]

Complete Information of Pramipexole Dihydrochloride


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