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Clinda-Derm - 0574-0016-02 - (Clindamycin Phosphate)

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Drug Information of Clinda-Derm

Product NDC: 0574-0016
Proprietary Name: Clinda-Derm
Non Proprietary Name: Clindamycin Phosphate
Active Ingredient(s): 10    mg/mL & nbsp;   Clindamycin Phosphate
Administration Route(s): TOPICAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Clinda-Derm

Product NDC: 0574-0016
Labeler Name: Paddock Laboratoratories, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA063329
Marketing Category: ANDA
Start Marketing Date: 19921001

Package Information of Clinda-Derm

Package NDC: 0574-0016-02
Package Description: 1 BOTTLE, WITH APPLICATOR in 1 CARTON (0574-0016-02) > 60 mL in 1 BOTTLE, WITH APPLICATOR

NDC Information of Clinda-Derm

NDC Code 0574-0016-02
Proprietary Name Clinda-Derm
Package Description 1 BOTTLE, WITH APPLICATOR in 1 CARTON (0574-0016-02) > 60 mL in 1 BOTTLE, WITH APPLICATOR
Product NDC 0574-0016
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clindamycin Phosphate
Dosage Form Name SOLUTION
Route Name TOPICAL
Start Marketing Date 19921001
Marketing Category Name ANDA
Labeler Name Paddock Laboratoratories, LLC
Substance Name CLINDAMYCIN PHOSPHATE
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes Decreased Sebaceous Gland Activity [PE],Lincosamide Antibacterial [EPC],Lincosamides [Chemical/Ingredient]

Complete Information of Clinda-Derm


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