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Sodium Bicarbonate - 50509-100-02 - (Sodium Bicarbonate)

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Drug Information of Sodium Bicarbonate

Product NDC: 50509-100
Proprietary Name: Sodium Bicarbonate
Non Proprietary Name: Sodium Bicarbonate
Active Ingredient(s): 1    meq/mL & nbsp;   Sodium Bicarbonate
Administration Route(s): PARENTERAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Sodium Bicarbonate

Product NDC: 50509-100
Labeler Name: Onpharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20100722

Package Information of Sodium Bicarbonate

Package NDC: 50509-100-02
Package Description: 4 CARTRIDGE in 1 CARTON (50509-100-02) > 2.7 mL in 1 CARTRIDGE (50509-100-01)

NDC Information of Sodium Bicarbonate

NDC Code 50509-100-02
Proprietary Name Sodium Bicarbonate
Package Description 4 CARTRIDGE in 1 CARTON (50509-100-02) > 2.7 mL in 1 CARTRIDGE (50509-100-01)
Product NDC 50509-100
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sodium Bicarbonate
Dosage Form Name SOLUTION
Route Name PARENTERAL
Start Marketing Date 20100722
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Onpharma, Inc.
Substance Name SODIUM BICARBONATE
Strength Number 1
Strength Unit meq/mL
Pharmaceutical Classes

Complete Information of Sodium Bicarbonate


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