Amoxicillin

Product NDC

21695-544

11-digit product format

216950544

Labeler code

21695

Product ID

21695-544_ee3875c6-5c49-4386-8ad2-5fe3208ed9e9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amoxicillin

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Rebel Distributors Corp.

Application

ANDA065228

Marketing category

ANDA

Marketing start

2005-07-13

Marketing end

0000-00-00

Substance

AMOXICILLIN

Active strength

875 mg/1

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record