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DEXAMETHASONE SODIUM PHOSPHATE - 0069-4543-02 - (DEXAMETHASONE SODIUM PHOSPHATE)

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Drug Information of DEXAMETHASONE SODIUM PHOSPHATE

Product NDC: 0069-4543
Proprietary Name: DEXAMETHASONE SODIUM PHOSPHATE
Non Proprietary Name: DEXAMETHASONE SODIUM PHOSPHATE
Active Ingredient(s): 4    mg/mL & nbsp;   DEXAMETHASONE SODIUM 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 PHOSPHATE

Product NDC: 0069-4543
Labeler Name: Pfizer Laboratories Div Pfizer Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040803
Marketing Category: ANDA
Start Marketing Date: 20110511

Package Information of DEXAMETHASONE SODIUM PHOSPHATE

Package NDC: 0069-4543-02
Package Description: 25 VIAL in 1 CARTON (0069-4543-02) > 5 mL in 1 VIAL (0069-4543-01)

NDC Information of DEXAMETHASONE SODIUM PHOSPHATE

NDC Code 0069-4543-02
Proprietary Name DEXAMETHASONE SODIUM PHOSPHATE
Package Description 25 VIAL in 1 CARTON (0069-4543-02) > 5 mL in 1 VIAL (0069-4543-01)
Product NDC 0069-4543
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DEXAMETHASONE SODIUM PHOSPHATE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; INTRAVENOUS; SOFT TISSUE
Start Marketing Date 20110511
Marketing Category Name ANDA
Labeler Name Pfizer Laboratories Div Pfizer Inc
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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