NDC 16729-232 – Ropinirole

Ropinirole Hydrochloride .25 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 7 recalls

Product NDC16729-232

Product details

Brand name
Ropinirole
Generic name
Ropinirole
Labeler
Accord Healthcare Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA204022
Marketed since
October 17, 2018
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
16729-232-01100 TABLET, FILM COATED in 1 BOTTLE (16729-232-01)Oct 17, 2018

Recalls mentioning this NDC

Other Ropinirole products