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Ropinirole Hydrochloride - 0615-7536-39 - (Ropinirole Hydrochloride)

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Drug Information of Ropinirole Hydrochloride

Product NDC: 0615-7536
Proprietary Name: Ropinirole Hydrochloride
Non Proprietary Name: Ropinirole Hydrochloride
Active Ingredient(s): .25    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: 0615-7536
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078881
Marketing Category: ANDA
Start Marketing Date: 20111027

Package Information of Ropinirole Hydrochloride

Package NDC: 0615-7536-39
Package Description: 30 TABLET in 1 BLISTER PACK (0615-7536-39)

NDC Information of Ropinirole Hydrochloride

NDC Code 0615-7536-39
Proprietary Name Ropinirole Hydrochloride
Package Description 30 TABLET in 1 BLISTER PACK (0615-7536-39)
Product NDC 0615-7536
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ropinirole Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111027
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name ROPINIROLE HYDROCHLORIDE
Strength Number .25
Strength Unit mg/1
Pharmaceutical Classes Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC]

Complete Information of Ropinirole Hydrochloride


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