AMOXICILLIN

Product NDC

61919-017

11-digit product format

619190017

Labeler code

61919

Product ID

61919-017_410c89e7-ce85-25ff-e054-00144ff88e88

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

AMOXICILLIN

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Direct Rx

Application

NDA050754

Marketing category

NDA

Marketing start

2014-01-01

Marketing end

0000-00-00

Substance

AMOXICILLIN

Active strength

875 mg/1

Pharmacologic classes

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

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record