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Neut Sodium Bicarbonate - 0409-6609-02 - (SODIUM BICARBONATE)

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Drug Information of Neut Sodium Bicarbonate

Product NDC: 0409-6609
Proprietary Name: Neut Sodium Bicarbonate
Non Proprietary Name: SODIUM BICARBONATE
Active Ingredient(s): .2    g/5mL & nbsp;   SODIUM BICARBONATE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Neut Sodium Bicarbonate

Product NDC: 0409-6609
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20050822

Package Information of Neut Sodium Bicarbonate

Package NDC: 0409-6609-02
Package Description: 25 VIAL in 1 TRAY (0409-6609-02) > 5 mL in 1 VIAL

NDC Information of Neut Sodium Bicarbonate

NDC Code 0409-6609-02
Proprietary Name Neut Sodium Bicarbonate
Package Description 25 VIAL in 1 TRAY (0409-6609-02) > 5 mL in 1 VIAL
Product NDC 0409-6609
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SODIUM BICARBONATE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20050822
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Hospira, Inc.
Substance Name SODIUM BICARBONATE
Strength Number .2
Strength Unit g/5mL
Pharmaceutical Classes

Complete Information of Neut Sodium Bicarbonate


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