Cephalexin

Product NDC
68788-9538
11-digit product format
687889538
Labeler code
68788
Product ID
68788-9538_8b197230-f3f8-48ac-9d94-b98a203dbd63
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Cephalexin
Dosage form
POWDER, FOR SUSPENSION
Route
ORAL
Labeler
Preferred Pharmaceuticals, Inc.
Application
ANDA062703
Marketing category
ANDA
Marketing start
2013-12-03
Marketing end
0000-00-00
Substance
CEPHALEXIN
Active strength
125 mg/5mL
Pharmacologic classes
Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68788-9538CEPHALEXIN POWDER, FOR SUSPENSION [PREFERRED PHARMACEUTICALS, INC.]10Legacy NDC20250223_07631a8b-eb84-46aa-844e-e93e548cb9b2.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68788-9538-168788953801100 mL in 1 BOTTLE (68788-9538-1) 100 ml2013-12-030000-00-00NoNoCurrent
68788-9538-268788953802200 mL in 1 BOTTLE (68788-9538-2) 200 ml2013-12-030000-00-00NoNoCurrent