NDC 50090-7445 – Ropinirole

Ropinirole Hydrochloride 4 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC50090-7445

Product details

Brand name
Ropinirole
Generic name
Ropinirole
Labeler
A-S Medication Solutions
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA079229
Marketed since
September 15, 2022
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
50090-7445-030 TABLET, FILM COATED in 1 BOTTLE (50090-7445-0)Nov 6, 2024

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