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Clindamycin - 17478-121-50 - (Clindamycin Phosphate)

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Drug Information of Clindamycin

Product NDC: 17478-121
Proprietary Name: Clindamycin
Non Proprietary Name: Clindamycin Phosphate
Active Ingredient(s): 600    mg/50mL & nbsp;   Clindamycin Phosphate
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Clindamycin

Product NDC: 17478-121
Labeler Name: Akorn, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA203048
Marketing Category: ANDA
Start Marketing Date: 20130405

Package Information of Clindamycin

Package NDC: 17478-121-50
Package Description: 1 BOTTLE, GLASS in 1 CARTON (17478-121-50) > 50 mL in 1 BOTTLE, GLASS

NDC Information of Clindamycin

NDC Code 17478-121-50
Proprietary Name Clindamycin
Package Description 1 BOTTLE, GLASS in 1 CARTON (17478-121-50) > 50 mL in 1 BOTTLE, GLASS
Product NDC 17478-121
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clindamycin Phosphate
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20130405
Marketing Category Name ANDA
Labeler Name Akorn, Inc.
Substance Name CLINDAMYCIN PHOSPHATE
Strength Number 600
Strength Unit mg/50mL
Pharmaceutical Classes Decreased Sebaceous Gland Activity [PE],Lincosamide Antibacterial [EPC],Lincosamides [Chemical/Ingredient]

Complete Information of Clindamycin


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