Cefdinir

Product NDC

68071-3393

11-digit product format

680713393

Labeler code

68071

Product ID

68071-3393_54c73290-bd6b-3453-e054-00144ff88e88

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cefdinir

Dosage form

POWDER, FOR SUSPENSION

Route

ORAL

Labeler

NuCare Pharmaceauticals,Inc.

Application

ANDA065429

Marketing category

ANDA

Marketing start

2013-10-04

Marketing end

0000-00-00

Substance

CEFDINIR MONOHYDRATE

Active strength

125 mg/5mL

Pharmacologic classes

Cephalosporin Antibacterial [EPC],Cephalosporins [CS]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record