NDC 50090-4684 – Ropinirole

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

Human Prescription Drug

Product NDC50090-4684

Product details

Brand name
Ropinirole
Generic name
Ropinirole
Labeler
A-S Medication Solutions
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090135
Marketed since
February 25, 2010
Listing expires
December 31, 2026
Pharmacologic class
Nonergot Dopamine Agonist

Active ingredients

Uses, dosage, side effects and warnings for Ropinirole →

Package NDC codes (2)

Package NDCDescriptionSince
50090-4684-030 TABLET, FILM COATED in 1 BOTTLE (50090-4684-0)Nov 5, 2019
50090-4684-190 TABLET, FILM COATED in 1 BOTTLE (50090-4684-1)Nov 5, 2019

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