NDC 62332-030 – Ropinirole

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

Human Prescription Drug

Product NDC62332-030

Product details

Brand name
Ropinirole
Generic name
Ropinirole
Labeler
Alembic Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090429
Marketed since
January 29, 2016
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
62332-030-31100 TABLET, FILM COATED in 1 BOTTLE (62332-030-31)Jan 29, 2016

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