NDC 60687-588 – Ropinirole hydrochloride

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

Human Prescription Drug

Product NDC60687-588

Product details

Brand name
Ropinirole hydrochloride
Generic name
Ropinirole hydrochloride
Labeler
American Health Packaging
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078110
Marketed since
June 9, 2021
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
60687-588-01100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-588-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-588-11)Jun 9, 2021

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