NDC 46708-265 – Ropinirole

Ropinirole Hydrochloride 8 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC46708-265

Product details

Brand name
Ropinirole
Generic name
Ropinirole
Labeler
Alembic Pharmaceuticals Limited
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA202786
Marketed since
March 14, 2013
Listing expires
December 31, 2026
Pharmacologic class
Nonergot Dopamine Agonist

Active ingredients

Uses, dosage, side effects and warnings for Ropinirole →

Package NDC codes (6)

Package NDCDescriptionSince
46708-265-10100 TABLET, FILM COATED, EXTENDED RELEASE in 1 CARTON (46708-265-10)Mar 14, 2013
46708-265-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-265-30)Mar 14, 2013
46708-265-31100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-265-31)Mar 14, 2013
46708-265-71500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-265-71)Mar 14, 2013
46708-265-9090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-265-90)Mar 14, 2013
46708-265-911000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-265-91)Mar 14, 2013

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