Chenodal
Chenodal 250 mg (chenodiol tablets)
Approved
Approval ID
b8b4539b-31d1-40cb-b284-86cf8b16522a
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 7, 2010
Manufacturers
FDA
Manchester Pharmaceuticals Inc.
DUNS: 832417641
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Chenodiol
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code45043-876
Application NumberANDA091019
Product Classification
M
Marketing Category
C73584
G
Generic Name
Chenodiol
Product Specifications
Route of AdministrationORAL
Effective DateJanuary 7, 2010
FDA Product Classification
INGREDIENTS (1)
ChenodiolActive
Quantity: 250 mg in 1 1
Code: 0GEI24LG0J
Classification: ACTIB