Details of the Drug Formulations

General Information of Drug (ID: DMHEAB1)

Drug Name
Neupro Drug Info
Synonyms
Rotigotine; 99755-59-6; Leganto; SPM 962; (S)-6-(propyl(2-(thiophen-2-yl)ethyl)amino)-5,6,7,8-tetrahydronaphthalen-1-ol; (6S)-rotigotine; UNII-87T4T8BO2E; (6S)-6-[propyl(2-thiophen-2-ylethyl)amino]-5,6,7,8-tetrahydronaphthalen-1-ol; SPM-962; N 0923; CHEMBL1303; 87T4T8BO2E; 99755-59-6 (free base); (6S)-6-(Propyl(2-(2-thienyl)ethyl)amino)-5,6,7,8-tetrahydro-1-naphthalenol; NCGC00168748-01; Rotigotine CDS Patch; (6s)-5,6,7,8-tetrahydro-6-[propyl[2-(2-thienyl)ethyl]amino]-1-naphthalenol; DSSTox_CID_26772; DSSTox_RID_81893; DSSTox_GSID_46772; C19H25NOS; Rotigotine CDS; (S)-5,6,7,8-Tetrahydro-6-(propyl(2-(2-thienyl)ethyl)amino)-1-naphthol; (S)-6-[Propyl-(2-thiophen-2-yl-ethyl)-amino]-5,6,7,8-tetrahydro-naphthalen-1-ol; CAS-99755-59-6; Neupro (TN); N-0923; Rotigotine [USAN:INN:BAN]; (S)-5,6,7,8-tetrahydro-6-[propyl[2-(2-thienyl)ethyl]amino]-1-naphthol; (S)-6-[Propyl[2-(thiophen-2-yl)ethyl]amino]-5,6,7,8-tetrahydronaphthalen-1-ol; SPM-936; SPM-937; PubChem16423; (-)-(S)-5,6,7,8-Tetrahydro-6-(propyl(2-(2-thienyl)ethyl)amino)-1-naphthol; GTPL941; cc-129; Rotigotine (JAN/USAN/INN); (-)-N-0437; SCHEMBL1088585; ZINC4028; DTXSID5046772; HSDB 8254; (2S)-2-[propyl-[2-(2-thienyl)ethyl]amino]tetralin-5-ol; CHEBI:135351; HMS3885D17; EX-A1164; Tox21_112627; 2696AH; BDBM50123626; MFCD00870193; s4274; AKOS016340728; Tox21_112627_1; AC-3547; CCG-267650; CS-0376; DB05271; SB19528; SS-4572; 1-naphthalenol, 5,6,7,8-tetrahydro-6-(propyl (2-(2-thienyl)ethyl)amino-(6S)-; NCGC00168748-02; HY-75502; AB0088886; SW220014-1; D05768; W-5179; 572R932; A846076; Q411985; J-502471; UNII-5QTR54Z0E1 component KFQYTPMOWPVWEJ-INIZCTEOSA-N; (6S)-6-(propyl-(2-thiophen-2-ylethyl)amino)-5,6,7,8-tetrahydronaphthalen-1-ol; 1-Naphthalenol, 5,6,7,8-tetrahydro-6-(propyl(2-(2-thienyl)ethyl)amino)-, (6S)-
Indication
Disease Entry ICD 11 Status REF
Restless legs syndrome 7A80 Phase 4 [1]
Parkinson disease 8A00.0 Phase 3 [2]
Cross-matching ID
PubChem CID
59227
ChEBI ID
CHEBI:135351
CAS Number
99755-59-6
TTD ID
D81KMY
ACDINA ID
D01405

Full List of Drug Formulations Containing This Drug

Rotigotine 1mg extended release film
Company Formulation ID FDA Description
Ucb F24135 Ascorbyl Palmitate; Povidone; Silicone Adhesive; Sodium Metabisulfite; Dl-Alphatocopherol
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Rotigotine 2mg extended release film
Company Formulation ID FDA Description
Ucb F24136 Ascorbyl Palmitate; Povidone; Silicone Adhesive; Sodium Metabisulfite; Dl-Alphatocopherol
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Rotigotine 3mg extended release film
Company Formulation ID FDA Description
Ucb F24137 Ascorbyl Palmitate; Povidone; Silicone Adhesive; Sodium Metabisulfite; Dl-Alphatocopherol
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Rotigotine 4mg extended release film
Company Formulation ID FDA Description
Ucb F24138 Ascorbyl Palmitate; Povidone; Silicone Adhesive; Sodium Metabisulfite; Dl-Alphatocopherol
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Rotigotine 6mg extended release film
Company Formulation ID FDA Description
Ucb F24139 Ascorbyl Palmitate; Povidone; Silicone Adhesive; Sodium Metabisulfite; Dl-Alphatocopherol
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Rotigotine 8mg extended release film
Company Formulation ID FDA Description
Ucb F24140 Ascorbyl Palmitate; Povidone; Silicone Adhesive; Sodium Metabisulfite; Dl-Alphatocopherol
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References

1 ClinicalTrials.gov (NCT01976871) Switching From Oral Dopamine Agonists to Rotigotine (SWITCH). U.S. National Institutes of Health.
2 ClinicalTrials.gov (NCT01723904) A Phase 3b, Open-Label, Safety and Efficacy Study of Rotigotine as Add-On Therapy With Low Doses of Pramipexole or Ropinirole in Patients With Advanced Parkinson's Disease. U.S. National Institutes of Health.