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Normosol-M and Dextrose - 0409-7965-09 - (DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, POTASSIUM ACETATE, and MAGNESIUM ACETATE)

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Drug Information of Normosol-M and Dextrose

Product NDC: 0409-7965
Proprietary Name: Normosol-M and Dextrose
Non Proprietary Name: DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, POTASSIUM ACETATE, and MAGNESIUM ACETATE
Active Ingredient(s): 5; 21; 128; 234    g/100mL; mg/100mL; mg/100mL; mg/100mL & nbsp;   DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, POTASSIUM ACETATE, and MAGNESIUM ACETATE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Normosol-M and Dextrose

Product NDC: 0409-7965
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA017610
Marketing Category: ANDA
Start Marketing Date: 20110906

Package Information of Normosol-M and Dextrose

Package NDC: 0409-7965-09
Package Description: 12 POUCH in 1 CASE (0409-7965-09) > 1 BAG in 1 POUCH > 1000 mL in 1 BAG

NDC Information of Normosol-M and Dextrose

NDC Code 0409-7965-09
Proprietary Name Normosol-M and Dextrose
Package Description 12 POUCH in 1 CASE (0409-7965-09) > 1 BAG in 1 POUCH > 1000 mL in 1 BAG
Product NDC 0409-7965
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, POTASSIUM ACETATE, and MAGNESIUM ACETATE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20110906
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name DEXTROSE MONOHYDRATE; MAGNESIUM ACETATE; POTASSIUM ACETATE; SODIUM CHLORIDE
Strength Number 5; 21; 128; 234
Strength Unit g/100mL; mg/100mL; mg/100mL; mg/100mL
Pharmaceutical Classes Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC],Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA]

Complete Information of Normosol-M and Dextrose


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