TobraDex - 0065-0647-10 - (tobramycin and dexamethasone)

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Drug Information of TobraDex

Product NDC: 0065-0647
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: 0065-0647
Labeler Name: Alcon Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050592
Marketing Category: NDA
Start Marketing Date: 19880915

Package Information of TobraDex

Package NDC: 0065-0647-10
Package Description: 10 mL in 1 BOTTLE, PLASTIC (0065-0647-10)

NDC Information of TobraDex

NDC Code 0065-0647-10
Proprietary Name TobraDex
Package Description 10 mL in 1 BOTTLE, PLASTIC (0065-0647-10)
Product NDC 0065-0647
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 Alcon Laboratories, Inc.
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


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