Cefaclor - 61442-175-01 - (Cefaclor)

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Drug Information of Cefaclor

Product NDC: 61442-175
Proprietary Name: Cefaclor
Non Proprietary Name: Cefaclor
Active Ingredient(s): 250    mg/5mL & nbsp;   Cefaclor
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Cefaclor

Product NDC: 61442-175
Labeler Name: Carlsbad Technology, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065412
Marketing Category: ANDA
Start Marketing Date: 20120327

Package Information of Cefaclor

Package NDC: 61442-175-01
Package Description: 150 mL in 1 BOTTLE, PLASTIC (61442-175-01)

NDC Information of Cefaclor

NDC Code 61442-175-01
Proprietary Name Cefaclor
Package Description 150 mL in 1 BOTTLE, PLASTIC (61442-175-01)
Product NDC 61442-175
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefaclor
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20120327
Marketing Category Name ANDA
Labeler Name Carlsbad Technology, Inc.
Substance Name CEFACLOR
Strength Number 250
Strength Unit mg/5mL
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cefaclor


General Information