NDC 0904-6374 – Ropinirole

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

Human Prescription Drug

Product NDC0904-6374

Product details

Brand name
Ropinirole
Generic name
Ropinirole
Labeler
Major Pharmaceuticals
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090429
Marketed since
October 1, 2014
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
0904-6374-61100 BLISTER PACK in 1 CARTON (0904-6374-61) / 1 TABLET, FILM COATED in 1 BLISTER PACKOct 1, 2014

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