Physiosol - 0409-6141-22 - (SODIUM CHLORIDE, SODIUM ACETATE ANHYDROUS, SODIUM GLUCONATE, POTASSIUM CHLORIDE, and MAGNESIUM CHLORIDE)

Alphabetical Index


Drug Information of Physiosol

Product NDC: 0409-6141
Proprietary Name: Physiosol
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): IRRIGATION
Dosage Form(s): IRRIGANT
Coding System: National Drug Codes(NDC)

Labeler Information of Physiosol

Product NDC: 0409-6141
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017637
Marketing Category: NDA
Start Marketing Date: 20110211

Package Information of Physiosol

Package NDC: 0409-6141-22
Package Description: 24 BOTTLE, PLASTIC in 1 CASE (0409-6141-22) > 250 mL in 1 BOTTLE, PLASTIC

NDC Information of Physiosol

NDC Code 0409-6141-22
Proprietary Name Physiosol
Package Description 24 BOTTLE, PLASTIC in 1 CASE (0409-6141-22) > 250 mL in 1 BOTTLE, PLASTIC
Product NDC 0409-6141
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SODIUM CHLORIDE, SODIUM ACETATE ANHYDROUS, SODIUM GLUCONATE, POTASSIUM CHLORIDE, and MAGNESIUM CHLORIDE
Dosage Form Name IRRIGANT
Route Name IRRIGATION
Start Marketing Date 20110211
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 Physiosol


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