Cefdinir

Product NDC

70518-2076

11-digit product format

705182076

Labeler code

70518

Product ID

70518-2076_8909cfeb-e97d-82b5-e053-2995a90a71b8

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cefdinir

Dosage form

POWDER, FOR SUSPENSION

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA065332

Marketing category

ANDA

Marketing start

2019-05-13

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