NDC 71335-0829 – Ropinirole Hydrochloride

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

Human Prescription Drug

Product NDC71335-0829

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
71335-0829-130 TABLET, FILM COATED in 1 BOTTLE (71335-0829-1)May 15, 2018
71335-0829-228 TABLET, FILM COATED in 1 BOTTLE (71335-0829-2)Jan 29, 2025
71335-0829-390 TABLET, FILM COATED in 1 BOTTLE (71335-0829-3)Jan 29, 2025
71335-0829-460 TABLET, FILM COATED in 1 BOTTLE (71335-0829-4)Jan 29, 2025
71335-0829-5100 TABLET, FILM COATED in 1 BOTTLE (71335-0829-5)Jan 29, 2025

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