Amoxicillin and Clavulanate Potassium

Product NDC

59115-024

11-digit product format

591150024

Labeler code

59115

Product ID

59115-024_b1204dff-4b55-4517-aa50-1cd70977cc37

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amoxicillin and Clavulanate Potassium

Dosage form

POWDER, FOR SUSPENSION

Route

ORAL

Labeler

Hikma Pharmaceutical

Application

ANDA065191

Marketing category

ANDA

Marketing start

2005-01-25

Marketing end

0000-00-00

Substance

AMOXICILLIN; CLAVULANATE POTASSIUM

Active strength

200 mg/5mL; mg/5mL

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record