NDC 72189-494 – Ropinirole

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

Human Prescription Drug

Product NDC72189-494

Product details

Brand name
Ropinirole
Generic name
Ropinirole
Labeler
Direct_Rx
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA079229
Marketed since
June 22, 2023
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
72189-494-3030 TABLET, FILM COATED in 1 BOTTLE (72189-494-30)Jun 22, 2023

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