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Sodium Bicarbonate - 0409-6637-34 - (SODIUM BICARBONATE)

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Drug Information of Sodium Bicarbonate

Product NDC: 0409-6637
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: 0409-6637
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 19840413

Package Information of Sodium Bicarbonate

Package NDC: 0409-6637-34
Package Description: 50 mL in 1 SYRINGE (0409-6637-34)

NDC Information of Sodium Bicarbonate

NDC Code 0409-6637-34
Proprietary Name Sodium Bicarbonate
Package Description 50 mL in 1 SYRINGE (0409-6637-34)
Product NDC 0409-6637
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SODIUM BICARBONATE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19840413
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Hospira, Inc.
Substance Name SODIUM BICARBONATE
Strength Number 84
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Sodium Bicarbonate


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