Active Ingredient: LITHIUM CARBONATE
Proprietary Name: LITHIUM CARBONATE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 300MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076170
Product Number: 001
Approval Date: Jun 10, 2002
Applicant Holder Full Name: HERITAGE PHARMA LABS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information