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Potassium Chloride in Dextrose - 0409-7905-09 - (DEXTROSE MONOHYDRATE and POTASSIUM CHLORIDE)

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Drug Information of Potassium Chloride in Dextrose

Product NDC: 0409-7905
Proprietary Name: Potassium Chloride in Dextrose
Non Proprietary Name: DEXTROSE MONOHYDRATE and POTASSIUM CHLORIDE
Active Ingredient(s): 5; .149    g/100mL; g/100mL & nbsp;   DEXTROSE MONOHYDRATE 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

Product NDC: 0409-7905
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA018371
Marketing Category: ANDA
Start Marketing Date: 19800529

Package Information of Potassium Chloride in Dextrose

Package NDC: 0409-7905-09
Package Description: 12 POUCH in 1 CASE (0409-7905-09) > 1 BAG in 1 POUCH > 1000 mL in 1 BAG

NDC Information of Potassium Chloride in Dextrose

NDC Code 0409-7905-09
Proprietary Name Potassium Chloride in Dextrose
Package Description 12 POUCH in 1 CASE (0409-7905-09) > 1 BAG in 1 POUCH > 1000 mL in 1 BAG
Product NDC 0409-7905
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DEXTROSE MONOHYDRATE and POTASSIUM CHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19800529
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name DEXTROSE MONOHYDRATE; POTASSIUM CHLORIDE
Strength Number 5; .149
Strength Unit g/100mL; g/100mL
Pharmaceutical Classes Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC]

Complete Information of Potassium Chloride in Dextrose


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