CEFDINIR

Product NDC

51655-019

11-digit product format

516550019

Labeler code

51655

Product ID

51655-019_de008247-b403-47fa-9ffd-f6667c17c934

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

CEFDINIR

Dosage form

CAPSULE

Route

ORAL

Labeler

Northwind Pharmaceuticals, LLC

Application

ANDA065330

Marketing category

ANDA

Marketing start

2015-02-10

Marketing end

0000-00-00

Substance

CEFDINIR

Active strength

300 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