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: A076382
Product Number: 001
Approval Date: Apr 21, 2003
Applicant Holder Full Name: ABLE LABORATORIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information