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Cleocin Pediatric - 0009-0760-04 - (clindamycin palmitate hydrochloride)

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Drug Information of Cleocin Pediatric

Product NDC: 0009-0760
Proprietary Name: Cleocin Pediatric
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 Pediatric

Product NDC: 0009-0760
Labeler Name: Pharmacia and Upjohn Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA061772
Marketing Category: ANDA
Start Marketing Date: 19710916

Package Information of Cleocin Pediatric

Package NDC: 0009-0760-04
Package Description: 75 mL in 1 BOTTLE (0009-0760-04)

NDC Information of Cleocin Pediatric

NDC Code 0009-0760-04
Proprietary Name Cleocin Pediatric
Package Description 75 mL in 1 BOTTLE (0009-0760-04)
Product NDC 0009-0760
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clindamycin palmitate hydrochloride
Dosage Form Name GRANULE, FOR SOLUTION
Route Name ORAL
Start Marketing Date 19710916
Marketing Category Name ANDA
Labeler Name Pharmacia and Upjohn Company
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 Pediatric


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