General MedicationsINJECTIONGeneric

CUPRIC SULFATE

Standard Dose

EQ 0.4MG COPPER/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 CUPRIC SULFATE is listed in Drugs@FDA under application 019350 (NDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient CUPRIC SULFATE Form and strength INJECTABLE;INJECTION - EQ 0.4MG COPPER/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor ABRAXIS PHARM Submission history Latest submission status date: 1992-06-09 00:00:00.

Structured Monograph

Clinical summary

Approval overview CUPRIC SULFATE is listed in Drugs@FDA under application 019350 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient CUPRIC SULFATE Form and strength INJECTABLE;INJECTION - EQ 0.4MG COPPER/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor ABRAXIS PHARM Submission history Latest submission status date: 1992-06-09 00:00:00. Submission type: SUPPL.

Monitoring

• Marketing status: Discontinued
• Review priority: STANDARD

Interaction Notes

No interaction notes stored yet.