Drugs@FDA: FDA Approved Drug Products

Home | Previous Page

New Drug Application (NDA): 201656
Company: ALYVANT
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
NOCTIVA DESMOPRESSIN ACETATE 0.00083MG/SPRAY SPRAY, METERED;NASAL Discontinued None Yes No
NOCTIVA DESMOPRESSIN ACETATE 0.00166MG/SPRAY SPRAY, METERED;NASAL Discontinued None Yes No
Original Approvals or Tentative Approvals
Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url
03/03/2017 ORIG-1 Approval Type 5 - New Formulation or New Manufacturer STANDARD Label (PDF)
Letter (PDF)
Review
Summary Review (PDF)
https://www.accessdata.fda.gov/drugsatfda_docs/label/2017/201656lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2017/201656Orig1s000Ltr.pdf https://www.accessdata.fda.gov/drugsatfda_docs/nda/2017/201656Orig1s000TOC.cfm https://www.accessdata.fda.gov/drugsatfda_docs/summary_review/2017/201656Orig1s000SumR.pdf
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels,
Patient Package Insert
Note Url
03/03/2017 ORIG-1 Approval Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2017/201656lbl.pdf

Note: If you need help accessing information in different file formats, see Instructions for Downloading Viewers and Players.
Language Assistance Available: Español | 繁體中文 | Tiếng Việt | 한국어 | Tagalog | Русский | العربية | Kreyòl Ayisyen | Français | Polski | Português | Italiano | Deutsch | 日本語 | فارسی | English