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ROPINIROLE HYDROCHLORIDE - 21695-792-60 - (ROPINIROLE HYDROCHLORIDE)

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Drug Information of ROPINIROLE HYDROCHLORIDE

Product NDC: 21695-792
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, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ROPINIROLE HYDROCHLORIDE

Product NDC: 21695-792
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078230
Marketing Category: ANDA
Start Marketing Date: 20080521

Package Information of ROPINIROLE HYDROCHLORIDE

Package NDC: 21695-792-60
Package Description: 60 TABLET, COATED in 1 BOTTLE, PLASTIC (21695-792-60)

NDC Information of ROPINIROLE HYDROCHLORIDE

NDC Code 21695-792-60
Proprietary Name ROPINIROLE HYDROCHLORIDE
Package Description 60 TABLET, COATED in 1 BOTTLE, PLASTIC (21695-792-60)
Product NDC 21695-792
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ROPINIROLE HYDROCHLORIDE
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20080521
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
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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