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General MedicationsSUBCUTANEOUSGeneric

LOVENOX (PRESERVATIVE FREE)

ENOXAPARIN SODIUM

Standard Dose
90MG/0.6ML (150MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Discontinued
Summary

Approval overview LOVENOX (PRESERVATIVE FREE) is listed in Drugs@FDA under application 020164 (NDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient ENOXAPARIN SODIUM Form and strength INJECTABLE;SUBCUTANEOUS - 90MG/0.6ML (150MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor SANOFI AVENTIS US Submission history Latest submission status date: 2023-07-28 00:00:00.

Structured Monograph

Clinical summary

Approval overview LOVENOX (PRESERVATIVE FREE) is listed in Drugs@FDA under application 020164 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient ENOXAPARIN SODIUM Form and strength INJECTABLE;SUBCUTANEOUS - 90MG/0.6ML (150MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor SANOFI AVENTIS US Submission history Latest submission status date: 2023-07-28 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Discontinued
  • • Review priority: STANDARD

Interaction Notes

  • No interaction notes stored yet.