UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
%
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
H H+ H1 HA HB HC HD HE HF HG HH HI HK HL HM HN HO HP HQ HR HS HT HU HV HX HY HZ
HPA HPH HPR HPT HPU HPV HPY

1(2H)-Phthalazinone, 4-((4-Chlorophenyl)methyl)-2-(hexahydro-1-methyl-1H-azepin-4-yl)-, Monohydrochloride

[The hydrochloride salt form of azelastine, a phthalazinone derivative with antihistaminergic activity. Azelastine hydrochloride competes with histamine for the H1 receptor, thereby diminishing the actions of histamine on effector cells and decreasing the histamine-mediated symptoms of allergic reaction, such as bronchoconstriction, vasodilation, increased capillary permeability and spasmodic contractions of gastrointestinal smooth muscle. ( NCI )]
UMLS (NCI) C0771004
Azelastine Hydrochloride
AZELASTINE HYDROCHLORIDE PREPARATION
W-2979M
 
Organic Chemical
Pharmacologic Substance
Relation/PAR: AZELASTINE
Relation/CHD: AZELASTINE HYDROCHLORIDE 0.05 %
AZELASTINE HYDROCHLORIDE 137 MCG/ACTUAT

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