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Sodium Bicarbonate - 0409-3486-16 - (SODIUM BICARBONATE)

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Drug Information of Sodium Bicarbonate

Product NDC: 0409-3486
Proprietary Name: Sodium Bicarbonate
Non Proprietary Name: SODIUM BICARBONATE
Active Ingredient(s): 75    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: 0409-3486
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077394
Marketing Category: ANDA
Start Marketing Date: 20120418

Package Information of Sodium Bicarbonate

Package NDC: 0409-3486-16
Package Description: 10 CARTON in 1 CONTAINER (0409-3486-16) > 1 SYRINGE, PLASTIC in 1 CARTON > 50 mL in 1 SYRINGE, PLASTIC

NDC Information of Sodium Bicarbonate

NDC Code 0409-3486-16
Proprietary Name Sodium Bicarbonate
Package Description 10 CARTON in 1 CONTAINER (0409-3486-16) > 1 SYRINGE, PLASTIC in 1 CARTON > 50 mL in 1 SYRINGE, PLASTIC
Product NDC 0409-3486
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SODIUM BICARBONATE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20120418
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name SODIUM BICARBONATE
Strength Number 75
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Sodium Bicarbonate


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