Clindesse - 64011-124-08 - (clindamycin phosphate)

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Drug Information of Clindesse

Product NDC: 64011-124
Proprietary Name: Clindesse
Non Proprietary Name: clindamycin phosphate
Active Ingredient(s): 20    mg/g & nbsp;   clindamycin phosphate
Administration Route(s): VAGINAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Clindesse

Product NDC: 64011-124
Labeler Name: Ther-Rx Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050793
Marketing Category: NDA
Start Marketing Date: 20091101

Package Information of Clindesse

Package NDC: 64011-124-08
Package Description: 5 g in 1 APPLICATOR (64011-124-08)

NDC Information of Clindesse

NDC Code 64011-124-08
Proprietary Name Clindesse
Package Description 5 g in 1 APPLICATOR (64011-124-08)
Product NDC 64011-124
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clindamycin phosphate
Dosage Form Name CREAM
Route Name VAGINAL
Start Marketing Date 20091101
Marketing Category Name NDA
Labeler Name Ther-Rx Corporation
Substance Name CLINDAMYCIN PHOSPHATE
Strength Number 20
Strength Unit mg/g
Pharmaceutical Classes Decreased Sebaceous Gland Activity [PE],Lincosamide Antibacterial [EPC],Lincosamides [Chemical/Ingredient]

Complete Information of Clindesse


General Information