NDC 55111-727 – Ropinirole

Ropinirole Hydrochloride 6 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC55111-727

Product details

Brand name
Ropinirole
Generic name
Ropinirole
Labeler
Dr. Reddys Laboratories Limited
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA201576
Marketed since
June 6, 2012
Listing expires
December 31, 2026
Pharmacologic class
Nonergot Dopamine Agonist

Active ingredients

Uses, dosage, side effects and warnings for Ropinirole →

Package NDC codes (3)

Package NDCDescriptionSince
55111-727-05500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-727-05)Jun 6, 2012
55111-727-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-727-30)Jun 6, 2012
55111-727-9090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-727-90)Jun 6, 2012

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