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Pramipexole - 57664-001-88 - (Pramipexole)

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Drug Information of Pramipexole

Product NDC: 57664-001
Proprietary Name: Pramipexole
Non Proprietary Name: Pramipexole
Active Ingredient(s): .125    mg/1 & nbsp;   Pramipexole
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Pramipexole

Product NDC: 57664-001
Labeler Name: Caraco Pharmaceutical Laboratories, Ltd.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091683
Marketing Category: ANDA
Start Marketing Date: 20130523

Package Information of Pramipexole

Package NDC: 57664-001-88
Package Description: 100 TABLET in 1 BOTTLE (57664-001-88)

NDC Information of Pramipexole

NDC Code 57664-001-88
Proprietary Name Pramipexole
Package Description 100 TABLET in 1 BOTTLE (57664-001-88)
Product NDC 57664-001
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pramipexole
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130523
Marketing Category Name ANDA
Labeler Name Caraco Pharmaceutical Laboratories, Ltd.
Substance Name PRAMIPEXOLE DIHYDROCHLORIDE
Strength Number .125
Strength Unit mg/1
Pharmaceutical Classes Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC]

Complete Information of Pramipexole


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