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Pramipexole Dihydrochloride - 0615-7597-39 - (Pramipexole Dihydrochloride)

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Drug Information of Pramipexole Dihydrochloride

Product NDC: 0615-7597
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: 0615-7597
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077724
Marketing Category: ANDA
Start Marketing Date: 20100101

Package Information of Pramipexole Dihydrochloride

Package NDC: 0615-7597-39
Package Description: 30 TABLET in 1 BLISTER PACK (0615-7597-39)

NDC Information of Pramipexole Dihydrochloride

NDC Code 0615-7597-39
Proprietary Name Pramipexole Dihydrochloride
Package Description 30 TABLET in 1 BLISTER PACK (0615-7597-39)
Product NDC 0615-7597
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pramipexole Dihydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100101
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
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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