Cefaclor - 61442-172-01 - (Cefaclor)

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Drug Information of Cefaclor

Product NDC: 61442-172
Proprietary Name: Cefaclor
Non Proprietary Name: Cefaclor
Active Ingredient(s): 500    mg/1 & nbsp;   Cefaclor
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Cefaclor

Product NDC: 61442-172
Labeler Name: Carlsbad Technology, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065146
Marketing Category: ANDA
Start Marketing Date: 20080731

Package Information of Cefaclor

Package NDC: 61442-172-01
Package Description: 100 CAPSULE in 1 BOTTLE, PLASTIC (61442-172-01)

NDC Information of Cefaclor

NDC Code 61442-172-01
Proprietary Name Cefaclor
Package Description 100 CAPSULE in 1 BOTTLE, PLASTIC (61442-172-01)
Product NDC 61442-172
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefaclor
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20080731
Marketing Category Name ANDA
Labeler Name Carlsbad Technology, Inc.
Substance Name CEFACLOR
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cefaclor


General Information