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
C C- C1 C3 C5 C6 C7 CA CB CC CD CE CF CG CH CI CJ CK CL CM CN CO CP CQ CR CS CT CU CV CW CX CY CZ
CA CA CA1 CA2 CA4 CAA CAB CAC CAD CAE CAF CAG CAH CAI CAL CAM CAN CAO CAP CAR CAS CAT CAU CAV CAY

Carbamic Acid,(10-(3-(4-morpholinyl)-1-oxopropyl)-10H-phenothiazin-2-yl)-, Ethyl Ester, Monohydrochloride

[The hydrochloride salt form of moricizine, a phenothiazine analog with class I antiarrhythmic activity. Moricizine hydrochloride blocks the rapid flow of sodium ions into the myocardial cell during phase 0 of the action potential. This decreases excitability, slows the impulse conduction through the atrioventricular (AV) node and depresses depolarization. ( NCI )]
UMLS (NCI) C0724636
Ethyl 10-(3-morpholinopropionyl)phenothiazine-2-carbamate hydrochloride
MORICIZINE HYDROCHLORIDE
MORICIZINE HYDROCHLORIDE PREPARATION
 
Organic Chemical
Pharmacologic Substance
Relation/PAR: MORICIZINE
Relation/CHD: MORICIZINE HYDROCHLORIDE 200 MG
MORICIZINE HYDROCHLORIDE 250 MG
MORICIZINE HYDROCHLORIDE 300 MG

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