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Dexamethasone Sodium Phosphates - 0517-4930-25 - (Dexamethasone Phosphate)

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Drug Information of Dexamethasone Sodium Phosphates

Product NDC: 0517-4930
Proprietary Name: Dexamethasone Sodium Phosphates
Non Proprietary Name: Dexamethasone Phosphate
Active Ingredient(s): 4    mg/mL & nbsp;   Dexamethasone Phosphate
Administration Route(s): INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; INTRAVENOUS; SOFT TISSUE
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Dexamethasone Sodium Phosphates

Product NDC: 0517-4930
Labeler Name: American Regent, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA087440
Marketing Category: ANDA
Start Marketing Date: 19900930

Package Information of Dexamethasone Sodium Phosphates

Package NDC: 0517-4930-25
Package Description: 25 VIAL, MULTI-DOSE in 1 BOX (0517-4930-25) > 30 mL in 1 VIAL, MULTI-DOSE

NDC Information of Dexamethasone Sodium Phosphates

NDC Code 0517-4930-25
Proprietary Name Dexamethasone Sodium Phosphates
Package Description 25 VIAL, MULTI-DOSE in 1 BOX (0517-4930-25) > 30 mL in 1 VIAL, MULTI-DOSE
Product NDC 0517-4930
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dexamethasone Phosphate
Dosage Form Name INJECTION, SOLUTION
Route Name INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; INTRAVENOUS; SOFT TISSUE
Start Marketing Date 19900930
Marketing Category Name ANDA
Labeler Name American Regent, Inc.
Substance Name DEXAMETHASONE PHOSPHATE
Strength Number 4
Strength Unit mg/mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Dexamethasone Sodium Phosphates


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