Amoxicillin and Clavulanate Potassium

Product NDC

68788-7155

11-digit product format

687887155

Labeler code

68788

Product ID

68788-7155_6e1ab320-5788-4576-8516-abb143fd960f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amoxicillin and Clavulanate Potassium

Dosage form

POWDER, FOR SUSPENSION

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA065066

Marketing category

ANDA

Marketing start

2018-05-09

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

2019-12-31

Current FDA listing

Historical FDA.report record