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Dexamethasone Sodium Phosphate - 24208-720-02 - (Dexamethasone Sodium Phosphate)

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Drug Information of Dexamethasone Sodium Phosphate

Product NDC: 24208-720
Proprietary Name: Dexamethasone Sodium Phosphate
Non Proprietary Name: Dexamethasone Sodium Phosphate
Active Ingredient(s): 1    mg/mL & nbsp;   Dexamethasone Sodium Phosphate
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Dexamethasone Sodium Phosphate

Product NDC: 24208-720
Labeler Name: Bausch & Lomb Incorporated
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040069
Marketing Category: ANDA
Start Marketing Date: 19960726

Package Information of Dexamethasone Sodium Phosphate

Package NDC: 24208-720-02
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (24208-720-02) > 5 mL in 1 BOTTLE, DROPPER

NDC Information of Dexamethasone Sodium Phosphate

NDC Code 24208-720-02
Proprietary Name Dexamethasone Sodium Phosphate
Package Description 1 BOTTLE, DROPPER in 1 CARTON (24208-720-02) > 5 mL in 1 BOTTLE, DROPPER
Product NDC 24208-720
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dexamethasone Sodium Phosphate
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 19960726
Marketing Category Name ANDA
Labeler Name Bausch & Lomb Incorporated
Substance Name DEXAMETHASONE SODIUM PHOSPHATE
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Dexamethasone Sodium Phosphate


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