amoxicillin and clavulanate potassium

Product NDC

68071-3250

11-digit product format

680713250

Labeler code

68071

Product ID

68071-3250_4f1f76fe-8169-384a-e054-00144ff88e88

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

amoxicillin and clavulanate potassium

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

NDA050720

Marketing category

NDA

Marketing start

1996-10-02

Marketing end

0000-00-00

Substance

AMOXICILLIN; CLAVULANATE POTASSIUM

Active strength

875 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