NDC 71335-2515 – Ropinirole

Ropinirole Hydrochloride 2 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-2515

Product details

Brand name
Ropinirole
Generic name
Ropinirole
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA079229
Marketed since
September 15, 2022
Listing expires
December 31, 2027
Pharmacologic class
Nonergot Dopamine Agonist

Active ingredients

Uses, dosage, side effects and warnings for Ropinirole →

Package NDC codes (3)

Package NDCDescriptionSince
71335-2515-130 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2515-1)Oct 24, 2024
71335-2515-260 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2515-2)Oct 24, 2024
71335-2515-390 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2515-3)Oct 24, 2024

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