Normosol-R - 0409-7967-03 - (SODIUM CHLORIDE, SODIUM ACETATE ANHYDROUS, SODIUM GLUCONATE, POTASSIUM CHLORIDE, AND MAGNESIUM CHLORIDE)

Alphabetical Index


Drug Information of Normosol-R

Product NDC: 0409-7967
Proprietary Name: Normosol-R
Non Proprietary Name: SODIUM CHLORIDE, SODIUM ACETATE ANHYDROUS, SODIUM GLUCONATE, POTASSIUM CHLORIDE, AND MAGNESIUM CHLORIDE
Active Ingredient(s): 30; 37; 222; 526; 502    mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL & nbsp;   SODIUM CHLORIDE, SODIUM ACETATE ANHYDROUS, SODIUM GLUCONATE, POTASSIUM CHLORIDE, AND MAGNESIUM CHLORIDE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Normosol-R

Product NDC: 0409-7967
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017586
Marketing Category: NDA
Start Marketing Date: 20100920

Package Information of Normosol-R

Package NDC: 0409-7967-03
Package Description: 24 POUCH in 1 CASE (0409-7967-03) > 1 BAG in 1 POUCH > 500 mL in 1 BAG

NDC Information of Normosol-R

NDC Code 0409-7967-03
Proprietary Name Normosol-R
Package Description 24 POUCH in 1 CASE (0409-7967-03) > 1 BAG in 1 POUCH > 500 mL in 1 BAG
Product NDC 0409-7967
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SODIUM CHLORIDE, SODIUM ACETATE ANHYDROUS, SODIUM GLUCONATE, POTASSIUM CHLORIDE, AND MAGNESIUM CHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20100920
Marketing Category Name NDA
Labeler Name Hospira, Inc.
Substance Name MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE ANHYDROUS; SODIUM CHLORIDE; SODIUM GLUCONATE
Strength Number 30; 37; 222; 526; 502
Strength Unit mg/100mL; mg/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-R


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