Application Nr Approved Date Route Status External Links
ANDA211624 None Intravenous None Google , Wikipedia , PubMed , DailyMed , Raw OpenFDA , ECHA , ToxNet , JECFA , FAO , 21 CFR

Indications and Purposes

1 Indications And Usage Fosaprepitant For Injection, In Combination With Other Antiemetic Agents, Is Indicated In Adults The Prevention Of: Acute And Delayed Nausea And Vomiting Associated With Initial And Repeat Courses Of Highly Emetogenic Cancer Chemotherapy (Hec) Including High-Dose Cisplatin. Delayed Nausea And Vomiting Associated With Initial And Repeat Courses Of Moderately Emetogenic Cancer Chemotherapy (Mec). Limitations Of Use Fosaprepitant Has Not Been Studied For The Treatment Of Established Nausea And Vomiting. Pediatric Use Information Is Approved For Merck Sharp & Dohme Corp., A Subsidiary Of Merck & Co., Inc.’s Emend (Fosaprepitant) For Injection. However, Due To Merck Sharp & Dohme Corp., A Subsidiary Of Merck & Co., Inc.’s Marketing Exclusivity Rights, This Drug Product Is Not Labeled With That Pediatric Information. Fosaprepitant For Injection Is A Substance P/neurokinin-1 (Nk 1 ) Receptor Antagonist, Indicated In Adults In Combination With Other Antiemetic Agents, For The Prevention Of ( 1 ): Acute And Delayed Nausea And Vomiting Associated With Initial And Repeat Courses Of Highly Emetogenic Cancer Chemotherapy (Hec) Including High-Dose Cisplatin. Delayed Nausea And Vomiting Associated With Initial And Repeat Courses Of Moderately Emetogenic Cancer Chemotherapy (Mec). Limitations Of Use ( 1 ) Fosaprepitant For Injection Has Not Been Studied For Treatment Of Established Nausea And Vomiting.

All Formulated Excipients (0 Total)

None

Active Ingredients ( 1 Total)

Name Structure ZINC ID(s)
1. Fosaprepitant Dimeglumine FOSAPREPITANT DIMEGLUMINE ZINC3939013

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