Cefdinir

Product NDC

68788-7255

11-digit product format

687887255

Labeler code

68788

Product ID

68788-7255_99f9b509-0cd7-480e-ad43-6137146503e6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cefdinir

Dosage form

POWDER, FOR SUSPENSION

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA065337

Marketing category

ANDA

Marketing start

2018-09-14

Marketing end

0000-00-00

Substance

CEFDINIR

Active strength

250 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