Amoxicillin

Product NDC

52959-296

11-digit product format

529590296

Labeler code

52959

Product ID

52959-296_7062e52f-035a-4d55-ba37-1b8ccc0ed7ef

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amoxicillin

Dosage form

POWDER, FOR SUSPENSION

Route

ORAL

Labeler

H.J. Harkins Company, Inc.

Application

ANDA065334

Marketing category

ANDA

Marketing start

2006-12-28

Marketing end

0000-00-00

Substance

AMOXICILLIN

Active strength

400 mg/5mL

Pharmacologic classes

Penicillin-class Antibacterial [EPC],Penicillins [CS]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record