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Sodium Bicarbonate - 63323-006-50 - (SODIUM BICARBONATE)

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Drug Information of Sodium Bicarbonate

Product NDC: 63323-006
Proprietary Name: Sodium Bicarbonate
Non Proprietary Name: SODIUM BICARBONATE
Active Ingredient(s): 84    mg/mL & nbsp;   SODIUM BICARBONATE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Sodium Bicarbonate

Product NDC: 63323-006
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20000810

Package Information of Sodium Bicarbonate

Package NDC: 63323-006-50
Package Description: 25 VIAL, SINGLE-DOSE in 1 TRAY (63323-006-50) > 50 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Sodium Bicarbonate

NDC Code 63323-006-50
Proprietary Name Sodium Bicarbonate
Package Description 25 VIAL, SINGLE-DOSE in 1 TRAY (63323-006-50) > 50 mL in 1 VIAL, SINGLE-DOSE
Product NDC 63323-006
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SODIUM BICARBONATE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20000810
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name APP Pharmaceuticals, LLC
Substance Name SODIUM BICARBONATE
Strength Number 84
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Sodium Bicarbonate


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