国家: 加拿大
语言: 英文
来源: Health Canada
CEFUROXIME (CEFUROXIME AXETIL)
NU-PHARM INC
J01DC02
CEFUROXIME
250MG
TABLET
CEFUROXIME (CEFUROXIME AXETIL) 250MG
ORAL
60/100/250
Prescription
SECOND GENERATION CEPHALOSPORINS
Active ingredient group (AIG) number: 0122448001; AHFS:
CANCELLED (UNRETURNED ANNUAL)
2018-03-28
Page 1 of 26 PRODUCT MONOGRAPH PR NU-CEFUROXIME CEFUROXIME AXETIL TABLETS 250 MG AND 500 MG CEFUROXIME/TABLET NU-PHARM STANDARD ANTIBIOTIC NU-PHARM INC. DATE OF PREPARATION: 50 MURAL ST., UNITS 1 & 2 OCTOBER 20, 2009 RICHMOND HILL, ONTARIO L4B 1E4 CONTROL#: 133377 Page 2 of 26 TABLE OF CONTENTS PART I: HEALTH PROFESSIONAL INFORMATION................................................................3 SUMMARY PRODUCT INFORMATION.................................................................................3 INDICATIONS AND CLINICAL USE.......................................................................................3 CONTRAINDICATIONS .......................................................................................................... 4 WARNINGS AND PRECAUTIONS.........................................................................................4 ADVERSE REACTIONS .........................................................................................................5 DRUG INTERACTIONS..........................................................................................................6 DOSAGE AND ADMINISTRATION.........................................................................................6 OVERDOSAGE....................................................................................................................... 7 ACTION AND CLINICAL PHARMACOLOGY .........................................................................7 STORAGE AND STABILITY ...................................................................................................7 DOSAGE FORMS, COMPOSITION AND PACKAGING ........................................................7 PART II: SCIENTIFIC INFORMATION.......................................................................................9 PHARMACEUTICAL INFORMATION.....................................................................................9 CLINICAL TRIALS....................................................................................................... 阅读完整的文件