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Sodium Bicarbonate - 0548-3352-00 - (Sodium Bicarbonate)

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Drug Information of Sodium Bicarbonate

Product NDC: 0548-3352
Proprietary Name: Sodium Bicarbonate
Non Proprietary Name: Sodium Bicarbonate
Active Ingredient(s): 84    mg/mL & nbsp;   Sodium Bicarbonate
Administration Route(s): PARENTERAL
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Sodium Bicarbonate

Product NDC: 0548-3352
Labeler Name: Amphastar Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20000601

Package Information of Sodium Bicarbonate

Package NDC: 0548-3352-00
Package Description: 10 SYRINGE in 1 CARTON (0548-3352-00) > 50 mL in 1 SYRINGE

NDC Information of Sodium Bicarbonate

NDC Code 0548-3352-00
Proprietary Name Sodium Bicarbonate
Package Description 10 SYRINGE in 1 CARTON (0548-3352-00) > 50 mL in 1 SYRINGE
Product NDC 0548-3352
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sodium Bicarbonate
Dosage Form Name INJECTION
Route Name PARENTERAL
Start Marketing Date 20000601
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Amphastar Pharmaceuticals, Inc.
Substance Name SODIUM BICARBONATE
Strength Number 84
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Sodium Bicarbonate


General Information