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
NDC Product Code45043-876
Application NumberANDA091019
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateJanuary 7, 2010
Generic NameChenodiol
INGREDIENTS (1)
ChenodiolActive
Quantity: 250 mg in 1 1
Code: 0GEI24LG0J
Classification: ACTIB