Amoxicillin and Clavulanate Potassium

Product NDC

70518-1267

11-digit product format

705181267

Labeler code

70518

Product ID

70518-1267_7266d83c-cea6-0d60-e053-2991aa0aa1f1

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amoxicillin and Clavulanate Potassium

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA091568

Marketing category

ANDA

Marketing start

2018-06-19

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