LITHIUM CARBONATE
Approved
Approval ID
75a54819-053b-4347-8b14-7b9ccc575042
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Apr 9, 2009
Manufacturers
FDA
STAT RX USA LLC
DUNS: 786036330
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
LITHIUM CARBONATE
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code16590-781
Application NumberNDA018558
Product Classification
M
Marketing Category
C73594
G
Generic Name
LITHIUM CARBONATE
Product Specifications
Route of AdministrationORAL
Effective DateApril 9, 2009
FDA Product Classification
INGREDIENTS (1)
LITHIUM CARBONATEActive
Quantity: 300 mg in 1 1
Code: 2BMD2GNA4V
Classification: ACTIB