Cefdinir - 54569-5917-0 - (Cefdinir)

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Drug Information of Cefdinir

Product NDC: 54569-5917
Proprietary Name: Cefdinir
Non Proprietary Name: Cefdinir
Active Ingredient(s): 250    mg/5mL & nbsp;   Cefdinir
Administration Route(s): ORAL
Dosage Form(s): POWDER, FOR SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Cefdinir

Product NDC: 54569-5917
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065429
Marketing Category: ANDA
Start Marketing Date: 20100806

Package Information of Cefdinir

Package NDC: 54569-5917-0
Package Description: 1 BOTTLE in 1 CARTON (54569-5917-0) > 60 mL in 1 BOTTLE

NDC Information of Cefdinir

NDC Code 54569-5917-0
Proprietary Name Cefdinir
Package Description 1 BOTTLE in 1 CARTON (54569-5917-0) > 60 mL in 1 BOTTLE
Product NDC 54569-5917
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefdinir
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20100806
Marketing Category Name ANDA
Labeler Name A-S Medication Solutions LLC
Substance Name CEFDINIR MONOHYDRATE
Strength Number 250
Strength Unit mg/5mL
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cefdinir


General Information