Amoxicillin and Clavulanate Potassium

Product NDC

55700-471

11-digit product format

557000471

Labeler code

55700

Product ID

55700-471_8cd5e71d-4ccc-4f33-b8cf-6c6208a5e48e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amoxicillin and Clavulanate Potassium

Dosage form

POWDER, FOR SUSPENSION

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA065162

Marketing category

ANDA

Marketing start

2004-09-23

Marketing end

0000-00-00

Substance

AMOXICILLIN; CLAVULANATE POTASSIUM

Active strength

600 mg/5mL; mg/5mL

Pharmacologic classes

beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA],Penicillin-class Antibacterial [EPC],Penicillins [CS]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record