NDC 67046-1490 – Ropinirole

Ropinirole Hydrochloride 3 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC67046-1490

Product details

Brand name
Ropinirole
Generic name
Ropinirole
Labeler
Coupler LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090429
Marketed since
January 29, 2025
Listing expires
December 31, 2026
Pharmacologic class
Nonergot Dopamine Agonist

Active ingredients

Uses, dosage, side effects and warnings for ropinirole →

Package NDC codes (1)

Package NDCDescriptionSince
67046-1490-330 TABLET, FILM COATED in 1 BLISTER PACK (67046-1490-3)Jan 29, 2025

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