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Potassium Chloride in Dextrose and Sodium Chloride - 0409-7107-09 - (DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE)

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Drug Information of Potassium Chloride in Dextrose and Sodium Chloride

Product NDC: 0409-7107
Proprietary Name: Potassium Chloride in Dextrose and Sodium Chloride
Non Proprietary Name: DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE
Active Ingredient(s): 50; 1.49; 9    g/1000mL; g/1000mL; g/1000mL & nbsp;   DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Potassium Chloride in Dextrose and Sodium Chloride

Product NDC: 0409-7107
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA019691
Marketing Category: ANDA
Start Marketing Date: 19880324

Package Information of Potassium Chloride in Dextrose and Sodium Chloride

Package NDC: 0409-7107-09
Package Description: 12 POUCH in 1 CASE (0409-7107-09) > 1 BAG in 1 POUCH > 1000 mL in 1 BAG

NDC Information of Potassium Chloride in Dextrose and Sodium Chloride

NDC Code 0409-7107-09
Proprietary Name Potassium Chloride in Dextrose and Sodium Chloride
Package Description 12 POUCH in 1 CASE (0409-7107-09) > 1 BAG in 1 POUCH > 1000 mL in 1 BAG
Product NDC 0409-7107
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19880324
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name DEXTROSE MONOHYDRATE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Strength Number 50; 1.49; 9
Strength Unit g/1000mL; g/1000mL; g/1000mL
Pharmaceutical Classes Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC]

Complete Information of Potassium Chloride in Dextrose and Sodium Chloride


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