LOTEMAX - 24208-299-05 - (loteprednol etabonate)

Alphabetical Index


Drug Information of LOTEMAX

Product NDC: 24208-299
Proprietary Name: LOTEMAX
Non Proprietary Name: loteprednol etabonate
Active Ingredient(s): 5    mg/mL & nbsp;   loteprednol etabonate
Administration Route(s): OPHTHALMIC
Dosage Form(s): SUSPENSION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of LOTEMAX

Product NDC: 24208-299
Labeler Name: Bausch & Lomb Incorporated
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020583
Marketing Category: NDA
Start Marketing Date: 19980309

Package Information of LOTEMAX

Package NDC: 24208-299-05
Package Description: 1 BOTTLE in 1 CARTON (24208-299-05) > 5 mL in 1 BOTTLE

NDC Information of LOTEMAX

NDC Code 24208-299-05
Proprietary Name LOTEMAX
Package Description 1 BOTTLE in 1 CARTON (24208-299-05) > 5 mL in 1 BOTTLE
Product NDC 24208-299
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name loteprednol etabonate
Dosage Form Name SUSPENSION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 19980309
Marketing Category Name NDA
Labeler Name Bausch & Lomb Incorporated
Substance Name LOTEPREDNOL ETABONATE
Strength Number 5
Strength Unit mg/mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of LOTEMAX


General Information