Chlorothiazide Oral Suspension

Brand(s)
Diuril
Category(s)
prescription
SPL Type(s)
Human Prescription
Master SPL
Salix Pharmaceuticals, Inc. (2013-05-31)
Oldest Current Product
1962-02-15
License(s)
NDA
RxNORM
ORAL SUSPENSION\CHLOROTHIAZIDE
FDAOB
ORAL\SUSPENSION\CHLOROTHIAZIDE
SPL Active
ORAL\SUSPENSION\CHLOROTHIAZIDE
SPL Moiety
ORAL\SUSPENSION\CHLOROTHIAZIDE

product(s) by strength(s)

chlorothiazide 50 mg/ml oral suspension

original product(s)(s)

#idbrandcategorylabelerfirst marketedactive ingredient(s)routedose formapplicationspl
1656490311DiurilNDASalix Pharmaceuticals, Inc.1962-02-15CHLOROTHIAZIDEORALSUSPENSIONNDA011870bd936e35-1af8-42da-bcc0-f22489d68574

application(s)

#idtitleapplicantapproved drug
1NDA011870DIURILSALIX PHARMACEUTICALS INCNDA011870_001

application drug(s)

#idcategory/deprecatedingredient strength(s)routedose formrldapplication
1NDA011870_001RXCHLOROTHIAZIDE (250MG/5ML)ORALSUSPENSIONTrueDIURIL

spl(s)

#idtitlecategorytypelabelerlast updateversionproduct(s)
1bd936e35-1af8-42da-bcc0-f22489d68574 (view SPL)DiurilprescriptionHuman PrescriptionSalix Pharmaceuticals, Inc.2013-05-3117656490311

Data from: FDAOB, FDAPB, LOINC, MTHSPL, NDFRT, NCIT, RxNORM, UNII