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ROPINIROLE HYDROCHLORIDE - 16590-734-90 - (ROPINIROLE HYDROCHLORIDE)

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Drug Information of ROPINIROLE HYDROCHLORIDE

Product NDC: 16590-734
Proprietary Name: ROPINIROLE HYDROCHLORIDE
Non Proprietary Name: ROPINIROLE HYDROCHLORIDE
Active Ingredient(s): 2    mg/1 & nbsp;   ROPINIROLE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of ROPINIROLE HYDROCHLORIDE

Product NDC: 16590-734
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078881
Marketing Category: ANDA
Start Marketing Date: 20090917

Package Information of ROPINIROLE HYDROCHLORIDE

Package NDC: 16590-734-90
Package Description: 90 TABLET in 1 BOTTLE (16590-734-90)

NDC Information of ROPINIROLE HYDROCHLORIDE

NDC Code 16590-734-90
Proprietary Name ROPINIROLE HYDROCHLORIDE
Package Description 90 TABLET in 1 BOTTLE (16590-734-90)
Product NDC 16590-734
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ROPINIROLE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090917
Marketing Category Name ANDA
Labeler Name STAT RX USA LLC
Substance Name ROPINIROLE HYDROCHLORIDE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC]

Complete Information of ROPINIROLE HYDROCHLORIDE


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