NDC 50090-4348 – Ropinirole hydrochloride

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

Human Prescription Drug

Product NDC50090-4348

Product details

Brand name
Ropinirole hydrochloride
Generic name
Ropinirole hydrochloride
Labeler
A-S Medication Solutions
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078110
Marketed since
September 20, 2011
Listing expires
December 31, 2027
Pharmacologic class
Nonergot Dopamine Agonist

Active ingredients

Uses, dosage, side effects and warnings for Ropinirole hydrochloride →

Package NDC codes (2)

Package NDCDescriptionSince
50090-4348-030 TABLET, FILM COATED in 1 BOTTLE (50090-4348-0)Jun 11, 2019
50090-4348-190 TABLET, FILM COATED in 1 BOTTLE (50090-4348-1)Jun 11, 2019

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