Zylet - 24208-358-05 - (loteprednol etabonate and tobramycin)

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Drug Information of Zylet

Product NDC: 24208-358
Proprietary Name: Zylet
Non Proprietary Name: loteprednol etabonate and tobramycin
Active Ingredient(s): 5; 3    mg/mL; mg/mL & nbsp;   loteprednol etabonate and tobramycin
Administration Route(s): OPHTHALMIC
Dosage Form(s): SUSPENSION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Zylet

Product NDC: 24208-358
Labeler Name: Bausch & Lomb Incorporated
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050804
Marketing Category: NDA
Start Marketing Date: 20041214

Package Information of Zylet

Package NDC: 24208-358-05
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (24208-358-05) > 5 mL in 1 BOTTLE, DROPPER

NDC Information of Zylet

NDC Code 24208-358-05
Proprietary Name Zylet
Package Description 1 BOTTLE, DROPPER in 1 CARTON (24208-358-05) > 5 mL in 1 BOTTLE, DROPPER
Product NDC 24208-358
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name loteprednol etabonate and tobramycin
Dosage Form Name SUSPENSION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 20041214
Marketing Category Name NDA
Labeler Name Bausch & Lomb Incorporated
Substance Name LOTEPREDNOL ETABONATE; TOBRAMYCIN
Strength Number 5; 3
Strength Unit mg/mL; mg/mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient]

Complete Information of Zylet


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