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ROPINIROLE HYDROCHLORIDE - 54868-5912-0 - (ROPINIROLE HYDROCHLORIDE)

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Drug Information of ROPINIROLE HYDROCHLORIDE

Product NDC: 54868-5912
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, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ROPINIROLE HYDROCHLORIDE

Product NDC: 54868-5912
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078230
Marketing Category: ANDA
Start Marketing Date: 20080627

Package Information of ROPINIROLE HYDROCHLORIDE

Package NDC: 54868-5912-0
Package Description: 30 TABLET, COATED in 1 BOTTLE, PLASTIC (54868-5912-0)

NDC Information of ROPINIROLE HYDROCHLORIDE

NDC Code 54868-5912-0
Proprietary Name ROPINIROLE HYDROCHLORIDE
Package Description 30 TABLET, COATED in 1 BOTTLE, PLASTIC (54868-5912-0)
Product NDC 54868-5912
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ROPINIROLE HYDROCHLORIDE
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20080627
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
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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