Drugs@FDA: FDA-Approved Drugs
New Drug Application (NDA): 214231
Company: ZEALAND PHARMA
Company: ZEALAND PHARMA
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
|---|---|---|---|---|---|---|---|
| ZEGALOGUE | DASIGLUCAGON HYDROCHLORIDE | EQ 0.6MG BASE/0.6ML (EQ 0.6MG BASE/0.6ML) | SOLUTION;SUBCUTANEOUS | Discontinued | None | Yes | No |
| ZEGALOGUE (AUTOINJECTOR) | DASIGLUCAGON HYDROCHLORIDE | EQ 0.6MG BASE/0.6ML (EQ 0.6MG BASE/0.6ML) | SOLUTION;SUBCUTANEOUS | 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 |
|---|---|---|---|---|---|---|---|
| 03/22/2021 | ORIG-1 | Approval | Type 1 - New Molecular Entity | STANDARD |
Label (PDF)
Letter (PDF) Review |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/214231s000lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2021/214231Orig1s000ltr.pdf https://www.accessdata.fda.gov/drugsatfda_docs/nda/2021/214231Orig1s000TOC.html |
| Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert |
Note | Url |
|---|---|---|---|---|---|
| 03/22/2021 | ORIG-1 | Approval | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/214231s000lbl.pdf |