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NDC 68788-8062-01 cefdinir 250 mg/5mL Details

cefdinir 250 mg/5mL

cefdinir is a ORAL POWDER, FOR SUSPENSION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is CEFDINIR.

MedlinePlus Drug Summary

Cefdinir is used to treat certain infections caused by bacteria such as bronchitis (infection of the airway tubes leading to the lungs); pneumonia; and infections of the skin, ears, sinuses, throat, and tonsils.. Cefdinir is in a class of medications called cephalosporin antibiotics. It works by killing bacteria. Antibiotics such as cefdinir will not work for colds, flu, or other viral infections. Using antibiotics when they are not needed increases your risk of getting an infection later that resists antibiotic treatment.

Related Packages: 68788-8062-01
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Cefdinir

Product Information

NDC	68788-8062
Product ID	68788-8062_d28ea6e9-e5af-4384-af05-a8b9d7f56644
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	cefdinir
Proprietary Name Suffix	n/a
Non-Proprietary Name	cefdinir
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	POWDER, FOR SUSPENSION
Route	ORAL
Active Ingredient Strength	250
Active Ingredient Units	mg/5mL
Substance Name	CEFDINIR
Labeler Name	Preferred Pharmaceuticals Inc.
Pharmaceutical Class	Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA210534
Listing Certified Through	2024-12-31

Package

NDC 68788-8062-01 (68788806201)

Pricing Information	N/A
NDC Package Code	68788-8062-1
Billing NDC	68788806201
Package	100 mL in 1 BOTTLE (68788-8062-1)
Marketing Start Date	2021-08-13
NDC Exclude Flag	N