Drugs@FDA: FDA-Approved Drugs
New Drug Application (NDA): 019999
Company: MERIDIAN MEDCL TECHN
Company: MERIDIAN MEDCL TECHN
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
|---|---|---|---|---|---|---|---|
| MORPHINE SULFATE (AUTOINJECTOR) | MORPHINE SULFATE | 10MG/0.7ML (10MG/0.7ML) | SOLUTION;INTRAMUSCULAR | Discontinued | None | Yes | No |
| Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert |
Note | Url |
|---|---|---|---|---|---|
| 10/07/2019 | SUPPL-23 | Labeling-Container/Carton Labels | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/019999s023lbl.pdf | |
| 10/07/2019 | SUPPL-23 | Labeling-Package Insert | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/019999s023lbl.pdf | |
| 12/16/2016 | SUPPL-22 | Labeling-Package Insert | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/019999s021s022lbl.pdf | |
| 12/16/2016 | SUPPL-21 | Labeling-Package Insert | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/019999s021s022lbl.pdf |