Amoxicillin and Clavulanate Potassium

Product NDC

68788-9055

11-digit product format

687889055

Labeler code

68788

Product ID

68788-9055_0bed6588-89b6-4536-bc92-fed4bc7bcbdb

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amoxicillin and Clavulanate Potassium

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA065101

Marketing category

ANDA

Marketing start

2012-01-25

Marketing end

0000-00-00

Substance

AMOXICILLIN; CLAVULANATE POTASSIUM

Active strength

500 mg/1; mg/1

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