Active Ingredient: LITHIUM CARBONATE
Proprietary Name: LITHIUM CARBONATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 300MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N016834
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PFIZER INC
Marketing Status:
Discontinued
Patent and Exclusivity Information