Amoxicillin

Product NDC

67253-146

11-digit product format

672530146

Labeler code

67253

Product ID

67253-146_0972267b-1a1b-40da-b95c-2dc7be21720e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amoxicillin

Dosage form

POWDER, FOR SUSPENSION

Route

ORAL

Labeler

DAVA Pharmaceuticals Inc

Application

ANDA065387

Marketing category

ANDA

Marketing start

2014-08-01

Marketing end

2020-02-29

Substance

AMOXICILLIN

Active strength

125 mg/5mL

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record