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General MedicationsINJECTIONGeneric

NAROPIN

ROPIVACAINE HYDROCHLORIDE

Standard Dose
50MG/10ML (5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 NAROPIN is listed in Drugs@FDA under application 020533 (NDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient ROPIVACAINE HYDROCHLORIDE Form and strength SOLUTION;INJECTION - 50MG/10ML (5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor FRESENIUS KABI USA Submission history Latest submission status date: 2022-06-28 00:00:00.

Structured Monograph

Clinical summary

Approval overview NAROPIN is listed in Drugs@FDA under application 020533 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient ROPIVACAINE HYDROCHLORIDE Form and strength SOLUTION;INJECTION - 50MG/10ML (5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor FRESENIUS KABI USA Submission history Latest submission status date: 2022-06-28 00:00:00. Submission type: SUPPL.

Monitoring

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

Interaction Notes

  • No interaction notes stored yet.