amoxicillin and clavulanate potassium

Product NDC

68788-9745

11-digit product format

687889745

Labeler code

68788

Product ID

68788-9745_4ad55e14-5f76-4248-8ecc-2d1980722abf

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

amoxicillin and clavulanate potassium

Dosage form

POWDER, FOR SUSPENSION

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

NDA050725

Marketing category

NDA

Marketing start

2012-09-25

Marketing end

0000-00-00

Substance

AMOXICILLIN; CLAVULANATE POTASSIUM

Active strength

400 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