Amoxicillin

Product NDC
50090-0858
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Amoxicillin
Dosage form
POWDER, FOR SUSPENSION
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA065325
Marketing category
ANDA
Substance
AMOXICILLIN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-0858-0100 mL in 1 BOTTLE (50090-0858-0) 2014-11-28NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
AmoxicillinA-S Medication Solutions2023-12-09HUMAN PRESCRIPTION DRUG LABEL17