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Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 217722
Company: HARM REDUCTION THERP
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
RIVIVE NALOXONE HYDROCHLORIDE 3MG/SPRAY SPRAY, METERED;NASAL Over-the-counter None Yes Yes
Original Approvals or Tentative Approvals
Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url
07/28/2023 ORIG-1 Approval Type 5 - New Formulation or New Manufacturer PRIORITY Label (PDF)
Letter (PDF)
Review
https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/217722Orig1s000Lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2023/217722Orig1s000ltr.pdf https://www.accessdata.fda.gov/drugsatfda_docs/nda/2023/217722Orig1s000TOC.cfm
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels,
Patient Package Insert
Note Url
07/28/2023 ORIG-1 Approval Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/217722Orig1s000Lbl.pdf

RIVIVE

The products listed here are over-the-counter (OTC) drugs and do not receive therapeutic equivalence ratings. They may not be interchangeable.

SPRAY, METERED;NASAL; 3MG/SPRAY
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD Application No. Company
RIVIVE NALOXONE HYDROCHLORIDE 3MG/SPRAY SPRAY, METERED;NASAL Over-the-counter Yes 217722 HARM REDUCTION THERP
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