Cefdinir - 0781-2176-64 - (Cefdinir)

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Drug Information of Cefdinir

Product NDC: 0781-2176
Proprietary Name: Cefdinir
Non Proprietary Name: Cefdinir
Active Ingredient(s): 300    mg/1 & nbsp;   Cefdinir
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Cefdinir

Product NDC: 0781-2176
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065330
Marketing Category: ANDA
Start Marketing Date: 20070406

Package Information of Cefdinir

Package NDC: 0781-2176-64
Package Description: 3 CARTON in 1 CARTON (0781-2176-64) > 1 BLISTER PACK in 1 CARTON > 10 CAPSULE in 1 BLISTER PACK

NDC Information of Cefdinir

NDC Code 0781-2176-64
Proprietary Name Cefdinir
Package Description 3 CARTON in 1 CARTON (0781-2176-64) > 1 BLISTER PACK in 1 CARTON > 10 CAPSULE in 1 BLISTER PACK
Product NDC 0781-2176
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefdinir
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20070406
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name CEFDINIR
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cefdinir


General Information