ETHNORUB

Main information

Trade name:
ETHNORUB 20G OINT

Active ingredient:
Methyl Salicylate,Mephenesin,Iodine

Available from:
Ethnor

Dosage:
4,5,0.5;%;W/W

Pharmaceutical form:
OINT

Composition:
20G

Medicine domain:
Humans

Medicine type:
Allopathic drug

Documents

for the general public:
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for healthcare professionals:
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Localization

Available in:
India

Language:
English

Other information

Status

Source:
Central Drugs Standard Control Organization

Last update:
09-08-2016

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13-6-2018

Orphan designation: N-tert-butyl-3-[(5-methyl-2-{[4-(2-pyrrolidin-1-ylethoxy)phenyl]amino}pyrimidin-4-yl)amino] benzenesulfonamide dihydrochloride monohydrate, for the: Treatment of post-essential thrombocythaemia myelofibrosis

Europe - EMA - European Medicines Agency

13-6-2018

Orphan designation: N-tert-butyl-3-[(5-methyl-2-{[4-(2-pyrrolidin-1-ylethoxy)phenyl]amino}pyrimidin-4-yl)amino] benzenesulfonamide dihydrochloride monohydrate, for the: Treatment of primary myelofibrosis

Europe - EMA - European Medicines Agency

13-6-2018

Orphan designation: N-tert-butyl-3-[(5-methyl-2-{[4-(2-pyrrolidin-1-ylethoxy)phenyl]amino}pyrimidin-4-yl)amino] benzenesulfonamide dihydrochloride monohydrate, for the: Treatment of post-polycythaemia vera myelofibrosis

Europe - EMA - European Medicines Agency

29-5-2018

Orphan designation: 2-[4-(1-methyl-4-pyridin-4-yl-1H-pyrazol-3-yl)-phenoxymethyl]-quinoline succinic acid, for the: Treatment of Huntington's disease

Europe - EMA - European Medicines Agency

3-5-2018

Orphan designation: (1'R,6'R)-3-(benzylamine)-6-hydroxy-3'-methyl-4-pentyl-6'-(prop-1-en-2-yl)-[1,1'-bi(cyclohexane)]-2',3,6-triene-2,5-dione, for the: Treatment of systemic sclerosis

Europe - EMA - European Medicines Agency

3-5-2018

Orphan designation: 6'-(R)-methyl-5-O-(5-amino-5,6-dideoxy-α-L-talofuranosyl)-paromamine sulfate, for the: Treatment of mucopolysaccharidosis type I

Europe - EMA - European Medicines Agency

3-5-2018

Orphan designation: 4-[[(1S,4S)-5-[[4-[4-(oxazol-2-yl)phenoxy]phenyl]methyl]-2,5-diazabicyclo[2.2.1]hept-2-yl]methyl]benzoic acid, for the: Treatment of cystic fibrosis

Europe - EMA - European Medicines Agency

29-6-2018

EU/3/18/2029 (Klinikum der UniversitAt MUnchen)

EU/3/18/2029 (Active substance: 2-[(2S)-2-methyl-1,4-dioxa-8-azaspiro[4.5]dec-8-yl]-8-nitro-6-trifluoromethyl-4H-1,3-benzothiazin-4-one) - Orphan designation - Commission Decision (2018)4174 of Fri, 29 Jun 2018 European Medicines Agency (EMA) procedure number: EMA/OD/004/18