Amoxicillin

Product NDC

33261-726

11-digit product format

332610726

Labeler code

33261

Product ID

33261-726_2c889e7d-281d-49ad-be10-1d316637583d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amoxicillin

Dosage form

POWDER, FOR SUSPENSION

Route

ORAL

Labeler

Aidarex Pharmaceuticals LLC

Application

ANDA065322

Marketing category

ANDA

Marketing start

2006-06-19

Marketing end

0000-00-00

Substance

AMOXICILLIN

Active strength

250 mg/5mL

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record