FDA
Lithium Citrate
The FDA lists this product in 4 strengths and forms.
Composition
- Active ingredients
- LITHIUM CITRATE EQ 300MG CARBONATE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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.
- LITHIUM CITRATE EQ 300MG CARBONATE/5ML · SyrupANDA217183-001 · Prescription
- LITHIUM CITRATE EQ 300MG CARBONATE/5ML · SyrupANDA218036-001 · Prescription
- LITHIUM CITRATE EQ 300MG CARBONATE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · SyrupThis page
- LITHIUM CITRATE EQ 300MG CARBONATE/5ML · SyrupANDA070755-001 · Prescription
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application NDA018421.
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
- Lithium Citrate
- Route
- Oral
- Dosage form
- Syrup
- Applicant
- Hikma
- Status
- Discontinued
- FDA approval
- 23 Dec 1980
- Application
- NDA018421-001