Amoxicillin and Clavulanate Potassium

Product NDC

68788-9316

11-digit product format

687889316

Labeler code

68788

Product ID

68788-9316_825f3ae0-0a14-49ef-9a61-15164039a7b4

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amoxicillin and Clavulanate Potassium

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA065064

Marketing category

ANDA

Marketing start

2015-04-13

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