NDC 0228-3661 – Ropinirole

Ropinirole Hydrochloride 12 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC0228-3661

Product details

Brand name
Ropinirole
Generic name
Ropinirole
Labeler
Actavis Pharma, Inc.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA090869
Marketed since
August 23, 2012
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
0228-3661-0330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0228-3661-03)Aug 23, 2012

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