Amoxicillin and Clavulanate Potassium

Product NDC

68071-4204

11-digit product format

680714204

Labeler code

68071

Product ID

68071-4204_617d0bad-7530-1b76-e053-2a91aa0a21d9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

amoxicillin and clavulanate potassium

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

NuCare Pharmaceuticals,Inc.

Application

ANDA065093

Marketing category

ANDA

Marketing start

2002-11-21

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