REQUIP 1 MG
ROPINIROLE (ROPINIROLE HYDROCHLORIDE) : 1 MG · DIN 02232567 · GLAXOSMITHKLINE INC
Health Canada status: CANCELLED POST MARKET
What is REQUIP?
REQUIP 1 MG contains ROPINIROLE (ROPINIROLE HYDROCHLORIDE) : 1 MG. It is listed in the Health Canada Drug Product Database under DIN 02232567, held by GLAXOSMITHKLINE INC, supplied as TABLET for ORAL administration. Health Canada currently lists it as cancelled post market, status dated 05-Mar-2018. Nexara Health is a licensed Canadian wholesale distributor (DEL 3-002896-A) and can source this product for hospitals, pharmacies and clinics. Availability and lead time are confirmed per order.
What is REQUIP used for?
Treatment of the signs and symptoms of idiopathic Parkinson's disease. Can be used as early therapy or as an adjunct to levodopa.
Authorized indication as written in the Health Canada product monograph. For healthcare professionals and licensed purchasers; this is not medical advice.
Product details and regulatory record
| DIN | 02232567 |
|---|---|
| Brand name | REQUIP |
| Generic / active ingredient | ROPINIROLE (ROPINIROLE HYDROCHLORIDE) : 1 MG |
| Manufacturer | GLAXOSMITHKLINE INC |
| Strength | 1 MG |
| Dosage form | TABLET |
| Route of administration | ORAL |
| Schedule | Prescription |
| ATC code | N04BC04 ROPINIROLE |
| AHFS class | 28:36.20.08 |
| Biosimilar | No |
| Health Canada status | CANCELLED POST MARKET |
| Status date | 05-Mar-2018 |
| Original market date | 1997-09-25 00:00:00 |
How is it administered?
Titrate dose to clinical response. Early therapy: start 0.25 mg t.i.d. Adjunct: reduce levodopa dose as Requip is increased. Max dose 24 mg/day. Discontinue gradually over 7 days.
Included because it drives pack selection and wastage. Consult the monograph.
How is it stored and handled?
Not specified in the provided text (refer to full monograph section STORAGE AND STABILITY).
How is it supplied?
Not explicitly detailed in provided text summary, but available in 0.25 mg, 1.0 mg, 2.0 mg, and 5.0 mg strengths.
Contraindications
Known hypersensitivity to ropinirole hydrochloride or any excipients in the drug product.
Warnings and precautions
Sudden onset of sleep without warning; orthostatic hypotension; hallucinations; impulse control disorders (gambling, hypersexuality); dyskinesia; potential for retinal pathology.
What can be used instead?
Other Canadian products sharing ATC code N04BC04 ROPINIROLE. 8 of 52 DINs in this group are currently marketed — marketed products are listed first, because that is what can actually be bought. These tables describe supply, not clinical equivalence: substitution rests with the prescriber or pharmacist, and interchangeability is determined provincially.
| Product | Strength | Form | Manufacturer | Health Canada status | DIN |
|---|---|---|---|---|---|
| SPC-ROPINIROLE | 0.25 MG | TABLET | SUN PHARMA CANADA INC | MARKETED | DIN 02314037 |
| SPC-ROPINIROLE | 1 MG | TABLET | SUN PHARMA CANADA INC | MARKETED | DIN 02314053 |
| SPC-ROPINIROLE | 2 MG | TABLET | SUN PHARMA CANADA INC | MARKETED | DIN 02314061 |
| SPC-ROPINIROLE | 5 MG | TABLET | SUN PHARMA CANADA INC | MARKETED | DIN 02314088 |
| TEVA-ROPINIROLE | 0.25 MG | TABLET | TEVA CANADA LIMITED | MARKETED | DIN 02316846 |
| TEVA-ROPINIROLE | 1 MG | TABLET | TEVA CANADA LIMITED | MARKETED | DIN 02316854 |
| TEVA-ROPINIROLE | 2 MG | TABLET | TEVA CANADA LIMITED | MARKETED | DIN 02316862 |
| TEVA-ROPINIROLE | 5 MG | TABLET | TEVA CANADA LIMITED | MARKETED | DIN 02316870 |
| APO-ROPINIROLE | 0.25 MG | TABLET | APOTEX INC | APPROVED | DIN 02337746 |
| APO-ROPINIROLE | 0.5 MG | TABLET | APOTEX INC | APPROVED | DIN 02337754 |
Who else supplies ROPINIROLE worldwide?
Nexara tracks national medicine registries and published price lists across multiple markets. ROPINIROLE appears in 2786 registered pack listings across 9 markets, published on 8 different national price bases. Where a Canadian route is closed, that is where an alternative route of supply starts — subject to the import rules in both countries.
Registered listings are not stock. Ask us to confirm what can actually be sourced for your order.
Can this still be bought in Canada?
No. This Drug Identification Number is cancelled post market in Health Canada's Drug Product Database, so the product is no longer authorized for sale in Canada and Nexara does not supply it. This page is kept as a regulatory record.
If you are looking for a current equivalent, the alternatives above list every product sharing this therapeutic class, with the marketed ones first. Ask us to source an alternative
Ordering questions
Who can buy this from Nexara?
Licensed entities only. Nexara holds Health Canada establishment licence DEL 3-002896-A and ships only to a licensed address.
Is there a minimum order?
Yes, set per product line and per pack multiple rather than on the order total, so you are never asked to buy a part-pack. The minimum for this line is confirmed with your quote.
What is the lead time?
Confirmed per order at quotation, and it depends on current stock position and whether the product is in shortage.
Can Nexara supply this for a clinical trial?
Yes — comparator and background-therapy supply, including sourcing from other markets where a Canadian pack will not satisfy the protocol. Clinical trial supply.