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Pramipexole dihydrochloride - 68462-331-05 - (Pramipexole dihydrochloride)

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Drug Information of Pramipexole dihydrochloride

Product NDC: 68462-331
Proprietary Name: Pramipexole dihydrochloride
Non Proprietary Name: Pramipexole dihydrochloride
Active Ingredient(s): .25    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: 68462-331
Labeler Name: Glenmark Generics Inc., USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090781
Marketing Category: ANDA
Start Marketing Date: 20101008

Package Information of Pramipexole dihydrochloride

Package NDC: 68462-331-05
Package Description: 500 TABLET in 1 BOTTLE (68462-331-05)

NDC Information of Pramipexole dihydrochloride

NDC Code 68462-331-05
Proprietary Name Pramipexole dihydrochloride
Package Description 500 TABLET in 1 BOTTLE (68462-331-05)
Product NDC 68462-331
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 Glenmark Generics Inc., USA
Substance Name PRAMIPEXOLE DIHYDROCHLORIDE
Strength Number .25
Strength Unit mg/1
Pharmaceutical Classes Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC]

Complete Information of Pramipexole dihydrochloride


General Information