FDA
Cupric Sulfate
The FDA lists this product in 3 strengths and forms.
Composition
- Active ingredients
- CUPRIC SULFATE EQ 0.4MG COPPER/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- CUPRIC SULFATE EQ 0.4MG COPPER/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · InjectableThis page
- CUPRIC SULFATE EQ 0.4MG COPPER/ML · InjectableANDA218745-001 · Discontinued
- CUPRIC SULFATE EQ 0.4MG COPPER/ML · InjectableANDA216324-001 · Prescription
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application NDA019350.
Prognia shows this product information for reference and learning. It is not treatment advice and can lag behind the official text. Always check the current product information and local protocols before prescribing.
At a glance
- Brand name
- Cupric Sulfate
- Route
- Injection
- Dosage form
- Injectable
- Applicant
- Abraxis Pharm
- Status
- Discontinued
- FDA approval
- 5 May 1987
- Application
- NDA019350-001