NDC 0615-8190 – Ropinirole Hydrochloride

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

Human Prescription Drug

Product NDC0615-8190

Product details

Brand name
Ropinirole Hydrochloride
Generic name
Ropinirole Hydrochloride
Labeler
NCS HealthCare of KY, LLC dba Vangard Labs
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 hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
0615-8190-3930 TABLET, FILM COATED in 1 BLISTER PACK (0615-8190-39)Mar 7, 2018

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