NDC 68788-4138 – Ropinirole

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

Human Prescription Drug

Product NDC68788-4138

Product details

Brand name
Ropinirole
Generic name
Ropinirole
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090135
Marketed since
July 6, 2026
Listing expires
December 31, 2027
Pharmacologic class
Nonergot Dopamine Agonist

Active ingredients

Uses, dosage, side effects and warnings for Ropinirole →

Package NDC codes (1)

Package NDCDescriptionSince
68788-4138-330 TABLET, FILM COATED in 1 BOTTLE (68788-4138-3)Jul 6, 2026

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