MORPHINE SULFATE (AUTOINJECTOR)
MORPHINE SULFATE
Approval overview MORPHINE SULFATE (AUTOINJECTOR) is listed in Drugs@FDA under application 019999 (NDA).
Review priority: STANDARD Marketing status: Discontinued Active ingredient MORPHINE SULFATE Form and strength SOLUTION;INTRAMUSCULAR - 10MG/0.7ML (10MG/0.7ML) Sponsor MERIDIAN MEDCL TECHN Submission history Latest submission status date: 2019-10-07 00:00:00.
Structured Monograph
Clinical summary
Approval overview MORPHINE SULFATE (AUTOINJECTOR) is listed in Drugs@FDA under application 019999 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient MORPHINE SULFATE Form and strength SOLUTION;INTRAMUSCULAR - 10MG/0.7ML (10MG/0.7ML) Sponsor MERIDIAN MEDCL TECHN Submission history Latest submission status date: 2019-10-07 00:00:00. Submission type: SUPPL.
Monitoring
- • Marketing status: Discontinued
- • Review priority: STANDARD
Interaction Notes
- No interaction notes stored yet.