Amoxicillin and Clavulanate Potassium

Product NDC

68788-6829

11-digit product format

687886829

Labeler code

68788

Product ID

68788-6829_847c7491-39d3-4ce9-9836-2534a576275f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amoxicillin and Clavulanate Potassium

Dosage form

SUSPENSION

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA065373

Marketing category

ANDA

Marketing start

2016-12-07

Marketing end

0000-00-00

Substance

AMOXICILLIN; CLAVULANATE POTASSIUM

Active strength

600 mg/5mL; mg/5mL

Pharmacologic classes

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

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record