cephalexin

Product NDC
50090-7091
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Cephalexin
Dosage form
FOR SUSPENSION
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA065234
Marketing category
ANDA
Substance
CEPHALEXIN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-7091-0200 mL in 1 BOTTLE (50090-7091-0) 2024-02-12NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
cephalexinA-S Medication Solutions2024-02-22HUMAN PRESCRIPTION DRUG LABEL1