NDC 71335-0727 – Ropinirole Hydrochloride

Ropinirole Hydrochloride .5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-0727

Product details

Brand name
Ropinirole Hydrochloride
Generic name
Ropinirole Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090429
Marketed since
January 29, 2016
Listing expires
December 31, 2026
Pharmacologic class
Nonergot Dopamine Agonist

Active ingredients

Uses, dosage, side effects and warnings for Ropinirole hydrochloride →

Package NDC codes (5)

Package NDCDescriptionSince
71335-0727-130 TABLET, FILM COATED in 1 BOTTLE (71335-0727-1)Feb 15, 2019
71335-0727-260 TABLET, FILM COATED in 1 BOTTLE (71335-0727-2)Mar 9, 2018
71335-0727-390 TABLET, FILM COATED in 1 BOTTLE (71335-0727-3)Aug 14, 2018
71335-0727-428 TABLET, FILM COATED in 1 BOTTLE (71335-0727-4)Oct 7, 2024
71335-0727-5100 TABLET, FILM COATED in 1 BOTTLE (71335-0727-5)Oct 7, 2024

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