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Pramipexole Dihydrochloride - 0555-0614-14 - (Pramipexole Dihydrochloride)

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Drug Information of Pramipexole Dihydrochloride

Product NDC: 0555-0614
Proprietary Name: Pramipexole Dihydrochloride
Non Proprietary Name: Pramipexole Dihydrochloride
Active Ingredient(s): 1    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: 0555-0614
Labeler Name: Barr Laboratories Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077724
Marketing Category: ANDA
Start Marketing Date: 20100104

Package Information of Pramipexole Dihydrochloride

Package NDC: 0555-0614-14
Package Description: 90 TABLET in 1 BOTTLE (0555-0614-14)

NDC Information of Pramipexole Dihydrochloride

NDC Code 0555-0614-14
Proprietary Name Pramipexole Dihydrochloride
Package Description 90 TABLET in 1 BOTTLE (0555-0614-14)
Product NDC 0555-0614
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pramipexole Dihydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100104
Marketing Category Name ANDA
Labeler Name Barr Laboratories Inc.
Substance Name PRAMIPEXOLE DIHYDROCHLORIDE
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC]

Complete Information of Pramipexole Dihydrochloride


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