Keflex

Product NDC

59630-115

11-digit product format

596300115

Labeler code

59630

Product ID

59630-115_f78e3c20-89a0-4a6f-ae60-d6285400bfc3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

cephalexin

Dosage form

CAPSULE

Route

ORAL

Labeler

Shionogi Inc.

Application

NDA050405

Marketing category

NDA

Marketing start

1971-01-04

Marketing end

0000-00-00

Substance

CEPHALEXIN

Active strength

750 mg/1

Pharmacologic classes

Cephalosporin Antibacterial [EPC],Cephalosporins [CS]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record