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Clindamycin - 55390-109-01 - (Clindamycin phosphate)

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Drug Information of Clindamycin

Product NDC: 55390-109
Proprietary Name: Clindamycin
Non Proprietary Name: Clindamycin phosphate
Active Ingredient(s): 150    mg/mL & nbsp;   Clindamycin phosphate
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Clindamycin

Product NDC: 55390-109
Labeler Name: Bedford Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065206
Marketing Category: ANDA
Start Marketing Date: 20050404

Package Information of Clindamycin

Package NDC: 55390-109-01
Package Description: 1 VIAL in 1 BOX, UNIT-DOSE (55390-109-01) > 60 mL in 1 VIAL

NDC Information of Clindamycin

NDC Code 55390-109-01
Proprietary Name Clindamycin
Package Description 1 VIAL in 1 BOX, UNIT-DOSE (55390-109-01) > 60 mL in 1 VIAL
Product NDC 55390-109
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clindamycin phosphate
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20050404
Marketing Category Name ANDA
Labeler Name Bedford Laboratories
Substance Name CLINDAMYCIN PHOSPHATE
Strength Number 150
Strength Unit mg/mL
Pharmaceutical Classes Decreased Sebaceous Gland Activity [PE],Lincosamide Antibacterial [EPC],Lincosamides [Chemical/Ingredient]

Complete Information of Clindamycin


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