Cefdinir

Product NDC

42043-251

11-digit product format

420430251

Labeler code

42043

Product ID

42043-251_4b67d33f-fefb-467e-aa10-a83f49ef2622

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cefdinir

Dosage form

POWDER, FOR SUSPENSION

Route

ORAL

Labeler

OrchidPharma Inc

Application

ANDA065429

Marketing category

ANDA

Marketing start

2013-10-04

Marketing end

2019-07-31

Substance

CEFDINIR MONOHYDRATE

Active strength

125 mg/5mL

Pharmacologic classes

Cephalosporin Antibacterial [EPC],Cephalosporins [CS]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record