NDC 87063-198 – Ropinirole

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

Human Prescription Drug

Product NDC87063-198

Product details

Brand name
Ropinirole
Generic name
Ropinirole
Labeler
ASCLEMED USA INC.
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 (4)

Package NDCDescriptionSince
87063-198-01100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-198-01)May 7, 2026
87063-198-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-198-30)May 7, 2026
87063-198-6060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-198-60)May 7, 2026
87063-198-9090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-198-90)May 7, 2026

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