MORPHINE SULFATE (AUTOINJECTOR) (MORPHINE SULFATE) — FDA Approval NDA019999 (MERIDIAN MEDCL TECHN)
MORPHINE SULFATE (AUTOINJECTOR) (MORPHINE SULFATE) — FDA Approval NDA019999 (MERIDIAN MEDCL TECHN) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: MORPHINE SULFATE (AUTOINJECTOR); Active ingredients: MORPHINE SULFATE; Application number: NDA019999.
| Brand name | MORPHINE SULFATE (AUTOINJECTOR) |
|---|---|
| Active ingredients | MORPHINE SULFATE |
| Application number | NDA019999 |
| Sponsor | MERIDIAN MEDCL TECHN |
| Dosage form | SOLUTION |
| Route | INTRAMUSCULAR |
| Marketing status | Discontinued |
| Products in application | 1 |
| First approval date | 19900712 |
| Source | openFDA Drugs@FDA |
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