NDC 71335-1188 – Ropinirole

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

Human Prescription Drug

Product NDC71335-1188

Product details

Brand name
Ropinirole
Generic name
Ropinirole
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA204022
Marketed since
October 17, 2018
Listing expires
December 31, 2026
Pharmacologic class
Nonergot Dopamine Agonist

Active ingredients

Uses, dosage, side effects and warnings for Ropinirole →

Package NDC codes (5)

Package NDCDescriptionSince
71335-1188-130 TABLET, FILM COATED in 1 BOTTLE (71335-1188-1)Mar 5, 2021
71335-1188-260 TABLET, FILM COATED in 1 BOTTLE (71335-1188-2)Apr 12, 2019
71335-1188-390 TABLET, FILM COATED in 1 BOTTLE (71335-1188-3)Oct 31, 2024
71335-1188-428 TABLET, FILM COATED in 1 BOTTLE (71335-1188-4)Oct 31, 2024
71335-1188-5100 TABLET, FILM COATED in 1 BOTTLE (71335-1188-5)Oct 31, 2024

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