Cefdinir

Product NDC

68788-6840

11-digit product format

687886840

Labeler code

68788

Product ID

68788-6840_589bcbbe-730c-4e5e-bdf2-ddaf574a5d95

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cefdinir

Dosage form

POWDER, FOR SUSPENSION

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA065429

Marketing category

ANDA

Marketing start

2016-12-06

Marketing end

0000-00-00

Substance

CEFDINIR MONOHYDRATE

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