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Pramipexole Dihydrochloride - 51079-577-20 - (pramipexole dihydrochloride)

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Drug Information of Pramipexole Dihydrochloride

Product NDC: 51079-577
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: 51079-577
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077854
Marketing Category: ANDA
Start Marketing Date: 20101117

Package Information of Pramipexole Dihydrochloride

Package NDC: 51079-577-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-577-20) > 1 TABLET in 1 BLISTER PACK (51079-577-01)

NDC Information of Pramipexole Dihydrochloride

NDC Code 51079-577-20
Proprietary Name Pramipexole Dihydrochloride
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-577-20) > 1 TABLET in 1 BLISTER PACK (51079-577-01)
Product NDC 51079-577
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name pramipexole dihydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101117
Marketing Category Name ANDA
Labeler Name UDL Laboratories, Inc.
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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