Active Ingredient: LITHIUM CARBONATE
Proprietary Name: LITHIUM CARBONATE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 450MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076366
Product Number: 001
Approval Date: Aug 21, 2003
Applicant Holder Full Name: HERITAGE PHARMA LABS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information