Cleocin - 54868-5833-0 - (clindamycin palmitate hydrochloride)

Alphabetical Index


Drug Information of Cleocin

Product NDC: 54868-5833
Proprietary Name: Cleocin
Non Proprietary Name: clindamycin palmitate hydrochloride
Active Ingredient(s): 75    mg/5mL & nbsp;   clindamycin palmitate hydrochloride
Administration Route(s): ORAL
Dosage Form(s): GRANULE, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cleocin

Product NDC: 54868-5833
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA061772
Marketing Category: ANDA
Start Marketing Date: 20071128

Package Information of Cleocin

Package NDC: 54868-5833-0
Package Description: 100 mL in 1 BOTTLE (54868-5833-0)

NDC Information of Cleocin

NDC Code 54868-5833-0
Proprietary Name Cleocin
Package Description 100 mL in 1 BOTTLE (54868-5833-0)
Product NDC 54868-5833
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clindamycin palmitate hydrochloride
Dosage Form Name GRANULE, FOR SOLUTION
Route Name ORAL
Start Marketing Date 20071128
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name CLINDAMYCIN PALMITATE HYDROCHLORIDE
Strength Number 75
Strength Unit mg/5mL
Pharmaceutical Classes Decreased Sebaceous Gland Activity [PE],Lincosamide Antibacterial [EPC],Lincosamides [Chemical/Ingredient]

Complete Information of Cleocin


General Information