Guanidine Oral Tablet

Category(s)
prescription
SPL Type(s)
Human Prescription
Master SPL
Merck Sharp & Dohme Corp. (2012-07-11)
Oldest Current Product
1939-10-02
License(s)
NDA
RxNORM
ORAL TABLET\GUANIDINE
FDAOB
ORAL\TABLET\GUANIDINE HYDROCHLORIDE
SPL Active
ORAL\TABLET\GUANIDINE HYDROCHLORIDE
SPL Moiety
ORAL\TABLET\GUANIDINE

product(s) by strength(s)

guanidine hydrochloride 125 mg oral tablet

original product(s)(s)

#idcategorylabelerfirst marketedactive ingredient(s)routedose formapplicationspl
1000850492NDAMerck Sharp & Dohme Corp.1939-10-02GUANIDINE HYDROCHLORIDEORALTABLETNDA001546903fbd33-e5d9-41fb-9414-7bd6f42a8593

application(s)

#idtitleapplicantapproved drug
1NDA001546GUANIDINE HYDROCHLORIDEMERCK SHARP AND DOHME CORPNDA001546_001

application drug(s)

#idcategory/deprecatedingredient strength(s)routedose formrldapplication
1NDA001546_001RXGUANIDINE HYDROCHLORIDE (125MG)ORALTABLETFalseGUANIDINE HYDROCHLORIDE

spl(s)

#idtitlecategorytypelabelerlabeler actlast updateversionproduct(s)
1903fbd33-e5d9-41fb-9414-7bd6f42a8593 (view SPL)GUANIDINEHYDROCHLORIDETabletsprescriptionHuman PrescriptionMerck Sharp & Dohme Corp.API MANUFACTURE, MANUFACTURE2012-07-112000850492

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