CEPHALEXIN
Approved
Approval ID
13831529-e814-4b95-9287-c5ba6678bf52
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Feb 22, 2010
Manufacturers
FDA
STAT RX USA LLC
DUNS: 786036330
Products 2
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
CEPHALEXIN
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code16590-051
Application NumberANDA065253
Product Classification
M
Marketing Category
C73584
G
Generic Name
CEPHALEXIN
Product Specifications
Route of AdministrationORAL
Effective DateFebruary 22, 2010
FDA Product Classification
INGREDIENTS (1)
CEPHALEXINActive
Quantity: 500 mg in 1 1
Code: OBN7UDS42Y
Classification: ACTIB
CEPHALEXIN
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code16590-050
Application NumberANDA065253
Product Classification
M
Marketing Category
C73584
G
Generic Name
CEPHALEXIN
Product Specifications
Route of AdministrationORAL
Effective DateFebruary 22, 2010
FDA Product Classification
INGREDIENTS (1)
CEPHALEXINActive
Quantity: 250 mg in 1 1
Code: OBN7UDS42Y
Classification: ACTIB