Cefdinir

Product NDC

68071-4236

11-digit product format

680714236

Labeler code

68071

Product ID

68071-4236_63026f19-2437-618b-e053-2a91aa0a9be0

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cefdinir

Dosage form

POWDER, FOR SUSPENSION

Route

ORAL

Labeler

NuCare Pharmaceuticals,Inc.

Application

ANDA065429

Marketing category

ANDA

Marketing start

2013-10-04

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