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PRAMIPEXOLE DIHYDROCHLORIDE - 68382-196-16 - (PRAMIPEXOLE DIHYDROCHLORIDE)

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Drug Information of PRAMIPEXOLE DIHYDROCHLORIDE

Product NDC: 68382-196
Proprietary Name: PRAMIPEXOLE DIHYDROCHLORIDE
Non Proprietary Name: PRAMIPEXOLE DIHYDROCHLORIDE
Active Ingredient(s): .125    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: 68382-196
Labeler Name: Zydus Pharmaceuticals (USA) Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078920
Marketing Category: ANDA
Start Marketing Date: 20100710

Package Information of PRAMIPEXOLE DIHYDROCHLORIDE

Package NDC: 68382-196-16
Package Description: 90 TABLET in 1 BOTTLE (68382-196-16)

NDC Information of PRAMIPEXOLE DIHYDROCHLORIDE

NDC Code 68382-196-16
Proprietary Name PRAMIPEXOLE DIHYDROCHLORIDE
Package Description 90 TABLET in 1 BOTTLE (68382-196-16)
Product NDC 68382-196
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PRAMIPEXOLE DIHYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100710
Marketing Category Name ANDA
Labeler Name Zydus Pharmaceuticals (USA) Inc.
Substance Name PRAMIPEXOLE DIHYDROCHLORIDE
Strength Number .125
Strength Unit mg/1
Pharmaceutical Classes Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC]

Complete Information of PRAMIPEXOLE DIHYDROCHLORIDE


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