CEFACLOR

Product NDC

59115-071

11-digit product format

591150071

Labeler code

59115

Product ID

59115-071_1ba7db86-11d0-4eb5-a4a1-96d7bf17523f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

CEFACLOR

Dosage form

CAPSULE

Route

ORAL

Labeler

Hikma Pharmaceutical

Application

ANDA065350

Marketing category

ANDA

Marketing start

2015-07-07

Marketing end

0000-00-00

Substance

CEFACLOR

Active strength

500 mg/1

Pharmacologic classes

Cephalosporin Antibacterial [EPC],Cephalosporins [CS]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record