Cefdinir - 65862-218-01 - (Cefdinir)

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Drug Information of Cefdinir

Product NDC: 65862-218
Proprietary Name: Cefdinir
Non Proprietary Name: Cefdinir
Active Ingredient(s): 125    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: 65862-218
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065473
Marketing Category: ANDA
Start Marketing Date: 20071214

Package Information of Cefdinir

Package NDC: 65862-218-01
Package Description: 1 BOTTLE in 1 CARTON (65862-218-01) > 100 mL in 1 BOTTLE

NDC Information of Cefdinir

NDC Code 65862-218-01
Proprietary Name Cefdinir
Package Description 1 BOTTLE in 1 CARTON (65862-218-01) > 100 mL in 1 BOTTLE
Product NDC 65862-218
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefdinir
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20071214
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name CEFDINIR
Strength Number 125
Strength Unit mg/5mL
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cefdinir


General Information