SUPRAX

Product NDC

70518-1020

11-digit product format

705181020

Labeler code

70518

Product ID

70518-1020_7d3f2562-8962-0e3c-e053-2a91aa0a9ddc

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

cefixime

Dosage form

CAPSULE

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

NDA203195

Marketing category

NDA

Marketing start

2018-02-16

Marketing end

0000-00-00

Substance

CEFIXIME

Active strength

400 mg/1

Pharmacologic classes

Cephalosporin Antibacterial [EPC],Cephalosporins [CS]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record