NDC 62332-107 – Ropinirole

Ropinirole Hydrochloride 2 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC62332-107

Product details

Brand name
Ropinirole
Generic name
Ropinirole
Labeler
Alembic Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA202786
Marketed since
June 20, 2020
Listing expires
December 31, 2027
Pharmacologic class
Nonergot Dopamine Agonist

Active ingredients

Uses, dosage, side effects and warnings for Ropinirole →

Package NDC codes (6)

Package NDCDescriptionSince
62332-107-10100 TABLET, FILM COATED, EXTENDED RELEASE in 1 CARTON (62332-107-10)Jun 20, 2020
62332-107-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62332-107-30)Jun 20, 2020
62332-107-31100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62332-107-31)Jun 20, 2020
62332-107-71500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62332-107-71)Jun 20, 2020
62332-107-9090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62332-107-90)Jun 20, 2020
62332-107-911000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62332-107-91)Jun 20, 2020

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