Amoxicillin and Clavulanate Potassium

Product NDC
68071-3864
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Amoxicillin and Clavulanate Potassium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA091568
Marketing category
ANDA
Substance
AMOXICILLIN; CLAVULANATE POTASSIUM
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
68071-3864-414 TABLET, FILM COATED in 1 BOTTLE (68071-3864-4) 2025-06-06NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Amoxicillin and Clavulanate PotassiumNuCare Pharmaceuticals,Inc.2025-06-06HUMAN PRESCRIPTION DRUG LABEL1