Active Ingredient: LITHIUM CARBONATE
Proprietary Name: LITHANE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 300MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N018833
Product Number: 001
Approval Date: Jul 18, 1985
Applicant Holder Full Name: BAYER PHARMACEUTICALS CORP
Marketing Status:
Discontinued
Patent and Exclusivity Information