Active Ingredient: LITHIUM CITRATE
Proprietary Name: LITHONATE
Dosage Form; Route of Administration: SYRUP; ORAL
Strength: EQ 300MG CARBONATE/5ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N017672
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: SOLVAY PHARMACEUTICALS
Marketing Status:
Discontinued
Patent and Exclusivity Information
