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Pramipexole Dihydrochloride - 65862-605-99 - (Pramipexole Dihydrochloride)

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Drug Information of Pramipexole Dihydrochloride

Product NDC: 65862-605
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: 65862-605
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202633
Marketing Category: ANDA
Start Marketing Date: 20121026

Package Information of Pramipexole Dihydrochloride

Package NDC: 65862-605-99
Package Description: 1000 TABLET in 1 BOTTLE (65862-605-99)

NDC Information of Pramipexole Dihydrochloride

NDC Code 65862-605-99
Proprietary Name Pramipexole Dihydrochloride
Package Description 1000 TABLET in 1 BOTTLE (65862-605-99)
Product NDC 65862-605
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pramipexole Dihydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20121026
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
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


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