Fosaprepitant

Product manufactured by Sandoz Inc.

Application Nr Approved Date Route Status External Links
ANDA212309 None Intravenous None Google , Wikipedia , PubMed , DailyMed , Raw OpenFDA , ECHA , ToxNet , JECFA , FAO , 21 CFR

Indications and Purposes

1 Indications & Usage Fosaprepitant For Injection, In Combination With Other Antiemetic Agents, Is Indicated In Adults For 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 For Injection 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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