NDC 72189-222 – Ropinirole

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

Human Prescription Drug

Product NDC72189-222

Product details

Brand name
Ropinirole
Generic name
Ropinirole
Labeler
DIRECT RX
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA204022
Marketed since
May 20, 2021
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
72189-222-3030 TABLET, FILM COATED in 1 BOTTLE (72189-222-30)May 20, 2021
72189-222-6060 TABLET, FILM COATED in 1 BOTTLE (72189-222-60)May 20, 2021

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