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: A076490
Product Number: 001
Approval Date: Jun 17, 2003
Applicant Holder Full Name: HIKMA INTERNATIONAL PHARMACEUTICALS LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information
