Cefdinir - 68180-722-20 - (Cefdinir)

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Drug Information of Cefdinir

Product NDC: 68180-722
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: 68180-722
Labeler Name: LUPIN PHARMACEUTICALS INC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065259
Marketing Category: ANDA
Start Marketing Date: 20070501

Package Information of Cefdinir

Package NDC: 68180-722-20
Package Description: 60 mL in 1 BOTTLE (68180-722-20)

NDC Information of Cefdinir

NDC Code 68180-722-20
Proprietary Name Cefdinir
Package Description 60 mL in 1 BOTTLE (68180-722-20)
Product NDC 68180-722
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefdinir
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20070501
Marketing Category Name ANDA
Labeler Name LUPIN PHARMACEUTICALS INC
Substance Name CEFDINIR
Strength Number 125
Strength Unit mg/5mL
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cefdinir


General Information