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PLASMA-LYTE 56 AND DEXTROSE - 0338-0147-03 - (Dextrose Monohydrate, Sodium Chloride, Potassium Acetate, Magnesium Acetate Tetrahydrate)

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Drug Information of PLASMA-LYTE 56 AND DEXTROSE

Product NDC: 0338-0147
Proprietary Name: PLASMA-LYTE 56 AND DEXTROSE
Non Proprietary Name: Dextrose Monohydrate, Sodium Chloride, Potassium Acetate, Magnesium Acetate Tetrahydrate
Active Ingredient(s): 5; 32; 128; 224    g/100mL; mg/100mL; mg/100mL; mg/100mL & nbsp;   Dextrose Monohydrate, Sodium Chloride, Potassium Acetate, Magnesium Acetate Tetrahydrate
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of PLASMA-LYTE 56 AND DEXTROSE

Product NDC: 0338-0147
Labeler Name: Baxter Healthcare Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017385
Marketing Category: NDA
Start Marketing Date: 19790201

Package Information of PLASMA-LYTE 56 AND DEXTROSE

Package NDC: 0338-0147-03
Package Description: 500 mL in 1 BAG (0338-0147-03)

NDC Information of PLASMA-LYTE 56 AND DEXTROSE

NDC Code 0338-0147-03
Proprietary Name PLASMA-LYTE 56 AND DEXTROSE
Package Description 500 mL in 1 BAG (0338-0147-03)
Product NDC 0338-0147
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dextrose Monohydrate, Sodium Chloride, Potassium Acetate, Magnesium Acetate Tetrahydrate
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 19790201
Marketing Category Name NDA
Labeler Name Baxter Healthcare Corporation
Substance Name DEXTROSE MONOHYDRATE; MAGNESIUM ACETATE TETRAHYDRATE; POTASSIUM ACETATE; SODIUM CHLORIDE
Strength Number 5; 32; 128; 224
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 PLASMA-LYTE 56 AND DEXTROSE


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