Amoxicillin

Product NDC

21695-294

11-digit product format

216950294

Labeler code

21695

Product ID

21695-294_5509ede4-74d3-42af-a1dd-cee95de5d2e6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amoxicillin

Dosage form

POWDER, FOR SUSPENSION

Route

ORAL

Labeler

Rebel Distributors Corp.

Application

ANDA065334

Marketing category

ANDA

Marketing start

2006-12-28

Marketing end

0000-00-00

Substance

AMOXICILLIN

Active strength

400 mg/5mL

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record