Amoxicillin

Product NDC

53217-316

11-digit product format

532170316

Labeler code

53217

Product ID

53217-316_eaf4eaa3-a21f-49d5-99da-1b7ee8795b9e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amoxicillin

Dosage form

POWDER, FOR SUSPENSION

Route

ORAL

Labeler

Aidarex Pharmaceuticals LLC

Application

ANDA065334

Marketing category

ANDA

Marketing start

2006-12-28

Marketing end

0000-00-00

Substance

AMOXICILLIN

Active strength

200 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