HEPARIN SODIUM
HEPARIN SODIUM
Approval overview HEPARIN SODIUM is listed in Drugs@FDA under application 017007 (NDA).
Review priority: STANDARD Marketing status: Discontinued Active ingredient HEPARIN SODIUM Form and strength INJECTABLE;INJECTION - 10,000 UNITS/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor HIKMA Submission history Latest submission status date: 2024-10-24 00:00:00.
Structured Monograph
Clinical summary
Approval overview HEPARIN SODIUM is listed in Drugs@FDA under application 017007 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient HEPARIN SODIUM Form and strength INJECTABLE;INJECTION - 10,000 UNITS/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor HIKMA Submission history Latest submission status date: 2024-10-24 00:00:00. Submission type: SUPPL.
Monitoring
- • Marketing status: Discontinued
- • Review priority: STANDARD
Interaction Notes
- No interaction notes stored yet.