TOBRADEX - 16590-223-25 - (TOBRAMYCIN and DEXAMETHASONE)

Alphabetical Index


Drug Information of TOBRADEX

Product NDC: 16590-223
Proprietary Name: TOBRADEX
Non Proprietary Name: TOBRAMYCIN and DEXAMETHASONE
Active Ingredient(s): 1; 3    mg/mL; mg/mL & nbsp;   TOBRAMYCIN and DEXAMETHASONE
Administration Route(s): OPHTHALMIC
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of TOBRADEX

Product NDC: 16590-223
Labeler Name: STAT Rx USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050592
Marketing Category: NDA
Start Marketing Date: 19880915

Package Information of TOBRADEX

Package NDC: 16590-223-25
Package Description: 2.5 mL in 1 BOTTLE, PLASTIC (16590-223-25)

NDC Information of TOBRADEX

NDC Code 16590-223-25
Proprietary Name TOBRADEX
Package Description 2.5 mL in 1 BOTTLE, PLASTIC (16590-223-25)
Product NDC 16590-223
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TOBRAMYCIN and DEXAMETHASONE
Dosage Form Name SUSPENSION
Route Name OPHTHALMIC
Start Marketing Date 19880915
Marketing Category Name NDA
Labeler Name STAT Rx USA LLC
Substance Name DEXAMETHASONE; TOBRAMYCIN
Strength Number 1; 3
Strength Unit mg/mL; mg/mL
Pharmaceutical Classes Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of TOBRADEX


General Information