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Sodium Phosphates - 0517-3415-25 - (sodium phosphate, monobasic, monohydrate and sodium phosphate, dibasic anhydrous)

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Drug Information of Sodium Phosphates

Product NDC: 0517-3415
Proprietary Name: Sodium Phosphates
Non Proprietary Name: sodium phosphate, monobasic, monohydrate and sodium phosphate, dibasic anhydrous
Active Ingredient(s): 142; 276    mg/mL; mg/mL & nbsp;   sodium phosphate, monobasic, monohydrate and sodium phosphate, dibasic anhydrous
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Sodium Phosphates

Product NDC: 0517-3415
Labeler Name: American Regent, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 19900930

Package Information of Sodium Phosphates

Package NDC: 0517-3415-25
Package Description: 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-3415-25) > 15 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Sodium Phosphates

NDC Code 0517-3415-25
Proprietary Name Sodium Phosphates
Package Description 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-3415-25) > 15 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0517-3415
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sodium phosphate, monobasic, monohydrate and sodium phosphate, dibasic anhydrous
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19900930
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name American Regent, Inc.
Substance Name SODIUM PHOSPHATE, DIBASIC ANHYDROUS; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE
Strength Number 142; 276
Strength Unit mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of Sodium Phosphates


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