Ropinirole — ingredient monograph

Overview

Source: NDC Directory

Ingredient name

ROPINIROLE HYDROCHLORIDE

Base moiety

ROPINIROLE

RxNorm CUI

799054

UNII

D7ZD41RZI9

Medication products

7

Brand names

3

Dosage forms

4

FAERS reports

18,695 · not a risk measure

Products containing this ingredient

Source: NDC Directory 7 products

Ropinirole 5% w/w Triturate with Lactose Powder
1 NDC
Ropinirole Hydrochloride Powder
7 NDC
Ropinirole Tablet, Extended Release
Rx ANDA TE AB 15 NDC
ropinirole Tablet, Film Coated
Rx ANDA TE AB 7 recalls 76 NDC
Ropinirole Tablet, Film Coated, Extended Release
Rx ANDA TE AB 20 NDC
ropinirole hydrochloride Tablet, Film Coated, Extended Release
Rx ANDA TE AB 5 NDC
ropinirole hydrochloride Tablet, Film Coated
Rx ANDA TE AB 33 NDC

Entries without a link are products listed by the FDA that carry no approval record, therapeutic equivalence rating or official labelling, so they have no detail page. Their facts are shown inline.

By dosage form

How this ingredient is presented across the catalogue.
Dosage form	Products	Examples
Powder	2	Ropinirole 5% w/w Triturate with Lactose, Ropinirole Hydrochloride
TABLET, Film Coated	2	ropinirole, ropinirole hydrochloride
TABLET, Film COATED, Extended Release	2	Ropinirole, ropinirole hydrochloride
TABLET, Extended Release	1	Ropinirole

Sources for this page

Dataset	Agency	Used for
NDC Directory	FDA	Ingredient name, strengths, products, labelers, packages
DailyMed RxNorm mappings	NLM	RxNorm concept identifier (RxCUI)
FAERS	FDA	Adverse event report totals