Amoxicillin and Clavulanate Potassium

Product NDC
72789-456
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Amoxicillin and Clavulanate Potassium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
PD-Rx Pharmaceuticals, Inc.
Application
ANDA091568
Marketing category
ANDA
Substance
AMOXICILLIN; CLAVULANATE POTASSIUM
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
72789-456-1414 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-456-14) 2024-12-11NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Amoxicillin and Clavulanate PotassiumPD-Rx Pharmaceuticals, Inc.2026-03-20HUMAN PRESCRIPTION DRUG LABEL24