NDC 10135-673 – Ropinirole

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

Human Prescription Drug

Product NDC10135-673

Product details

Brand name
Ropinirole
Generic name
Ropinirole
Labeler
Marlex Pharmaceuticals Inc
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA079165
Marketed since
March 15, 2019
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
10135-673-01100 TABLET, FILM COATED in 1 BOTTLE (10135-673-01)Mar 15, 2019

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