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clindamycin phosphate - 59762-3743-1 - (clindamycin phosphate)

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Drug Information of clindamycin phosphate

Product NDC: 59762-3743
Proprietary Name: clindamycin phosphate
Non Proprietary Name: clindamycin phosphate
Active Ingredient(s): 10    mg/g & nbsp;   clindamycin phosphate
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of clindamycin phosphate

Product NDC: 59762-3743
Labeler Name: Greenstone LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050615
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 19870107

Package Information of clindamycin phosphate

Package NDC: 59762-3743-1
Package Description: 30 g in 1 TUBE (59762-3743-1)

NDC Information of clindamycin phosphate

NDC Code 59762-3743-1
Proprietary Name clindamycin phosphate
Package Description 30 g in 1 TUBE (59762-3743-1)
Product NDC 59762-3743
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clindamycin phosphate
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 19870107
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Greenstone LLC
Substance Name CLINDAMYCIN PHOSPHATE
Strength Number 10
Strength Unit mg/g
Pharmaceutical Classes Decreased Sebaceous Gland Activity [PE],Lincosamide Antibacterial [EPC],Lincosamides [Chemical/Ingredient]

Complete Information of clindamycin phosphate


General Information