AMOXICILLIN AND CLAVULANATE POTASSIUM

Product NDC
68071-3774
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
amoxicillin and clavulanate potassium
Dosage form
FOR SUSPENSION
Route
ORAL
Labeler
NuCare Pharmaceuticals, Inc.
Application
NDA050755
Marketing category
NDA AUTHORIZED GENERIC
Substance
AMOXICILLIN; CLAVULANATE POTASSIUM
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
68071-3774-5125 mL in 1 BOTTLE (68071-3774-5) 2025-01-14NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
AMOXICILLIN AND CLAVULANATE POTASSIUMNuCare Pharmaceuticals, Inc.2025-01-14HUMAN PRESCRIPTION DRUG LABEL1