NDC 69452-357 – Ropinirole

Ropinirole Hydrochloride .5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC69452-357

Product details

Brand name
Ropinirole
Generic name
Ropinirole
Labeler
Bionpharma 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 (1)

Package NDCDescriptionSince
69452-357-20100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69452-357-20)Sep 15, 2022

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