VELTIN - 0145-0071-01 - (clindamycin phosphate and tretinoin)

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Drug Information of VELTIN

Product NDC: 0145-0071
Proprietary Name: VELTIN
Non Proprietary Name: clindamycin phosphate and tretinoin
Active Ingredient(s): 10; .25    mg/g; mg/g & nbsp;   clindamycin phosphate and tretinoin
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of VELTIN

Product NDC: 0145-0071
Labeler Name: Stiefel Laboratories Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050803
Marketing Category: NDA
Start Marketing Date: 20100729

Package Information of VELTIN

Package NDC: 0145-0071-01
Package Description: 10 TUBE in 1 CARTON (0145-0071-01) > 2 g in 1 TUBE (0145-0071-03)

NDC Information of VELTIN

NDC Code 0145-0071-01
Proprietary Name VELTIN
Package Description 10 TUBE in 1 CARTON (0145-0071-01) > 2 g in 1 TUBE (0145-0071-03)
Product NDC 0145-0071
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clindamycin phosphate and tretinoin
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20100729
Marketing Category Name NDA
Labeler Name Stiefel Laboratories Inc
Substance Name CLINDAMYCIN PHOSPHATE; TRETINOIN
Strength Number 10; .25
Strength Unit mg/g; mg/g
Pharmaceutical Classes Decreased Sebaceous Gland Activity [PE],Lincosamide Antibacterial [EPC],Lincosamides [Chemical/Ingredient],Retinoid [EPC],Retinoids [Chemical/Ingredient]

Complete Information of VELTIN


General Information