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Dexamethasone Sodium Phosphate - 63323-165-30 - (DEXAMETHASONE SODIUM PHOSPHATE)

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Drug Information of Dexamethasone Sodium Phosphate

Product NDC: 63323-165
Proprietary Name: Dexamethasone Sodium Phosphate
Non Proprietary Name: DEXAMETHASONE SODIUM PHOSPHATE
Active Ingredient(s): 4    mg/mL & nbsp;   DEXAMETHASONE SODIUM PHOSPHATE
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Dexamethasone Sodium Phosphate

Product NDC: 63323-165
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084916
Marketing Category: ANDA
Start Marketing Date: 20000907

Package Information of Dexamethasone Sodium Phosphate

Package NDC: 63323-165-30
Package Description: 1 VIAL, MULTI-DOSE in 1 BOX (63323-165-30) > 30 mL in 1 VIAL, MULTI-DOSE

NDC Information of Dexamethasone Sodium Phosphate

NDC Code 63323-165-30
Proprietary Name Dexamethasone Sodium Phosphate
Package Description 1 VIAL, MULTI-DOSE in 1 BOX (63323-165-30) > 30 mL in 1 VIAL, MULTI-DOSE
Product NDC 63323-165
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DEXAMETHASONE SODIUM PHOSPHATE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20000907
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name DEXAMETHASONE SODIUM PHOSPHATE
Strength Number 4
Strength Unit mg/mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Dexamethasone Sodium Phosphate


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