Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 019367

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POTASSIUM CHLORIDE 10MEQ IN DEXTROSE 5% AND LACTATED RINGER'S IN PLASTIC CONTAINER (CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE)
20MG/100ML;5GM/100ML;105MG/100ML;600MG/100ML;310MG/100ML
Marketing Status: Prescription

Active Ingredient: CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE
Proprietary Name: POTASSIUM CHLORIDE 10MEQ IN DEXTROSE 5% AND LACTATED RINGER'S IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 20MG/100ML;5GM/100ML;105MG/100ML;600MG/100ML;310MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N019367
Product Number: 002
Approval Date: Apr 5, 1985
Applicant Holder Full Name: BAXTER HEALTHCARE CORP
Marketing Status:  Prescription
Patent and Exclusivity Information

POTASSIUM CHLORIDE 10MEQ IN DEXTROSE 5% AND LACTATED RINGER'S IN PLASTIC CONTAINER (CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE)
20MG/100ML;5GM/100ML;179MG/100ML;600MG/100ML;310MG/100ML
Marketing Status: Prescription

Active Ingredient: CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE
Proprietary Name: POTASSIUM CHLORIDE 10MEQ IN DEXTROSE 5% AND LACTATED RINGER'S IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 20MG/100ML;5GM/100ML;179MG/100ML;600MG/100ML;310MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N019367
Product Number: 003
Approval Date: Apr 5, 1985
Applicant Holder Full Name: BAXTER HEALTHCARE CORP
Marketing Status:  Prescription
Patent and Exclusivity Information

POTASSIUM CHLORIDE 15MEQ IN DEXTROSE 5% AND LACTATED RINGER'S IN PLASTIC CONTAINER (CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE)
20MG/100ML;5GM/100ML;254MG/100ML;600MG/100ML;310MG/100ML
Marketing Status: Prescription

Active Ingredient: CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE
Proprietary Name: POTASSIUM CHLORIDE 15MEQ IN DEXTROSE 5% AND LACTATED RINGER'S IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 20MG/100ML;5GM/100ML;254MG/100ML;600MG/100ML;310MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: N019367
Product Number: 006
Approval Date: Apr 5, 1985
Applicant Holder Full Name: BAXTER HEALTHCARE CORP
Marketing Status:  Prescription
Patent and Exclusivity Information

POTASSIUM CHLORIDE 20MEQ IN DEXTROSE 5% AND LACTATED RINGER'S IN PLASTIC CONTAINER (CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE)
20MG/100ML;5GM/100ML;179MG/100ML;600MG/100ML;310MG/100ML
Marketing Status: Prescription

Active Ingredient: CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE
Proprietary Name: POTASSIUM CHLORIDE 20MEQ IN DEXTROSE 5% AND LACTATED RINGER'S IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 20MG/100ML;5GM/100ML;179MG/100ML;600MG/100ML;310MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: N019367
Product Number: 004
Approval Date: Apr 5, 1985
Applicant Holder Full Name: BAXTER HEALTHCARE CORP
Marketing Status:  Prescription
Patent and Exclusivity Information

POTASSIUM CHLORIDE 20MEQ IN DEXTROSE 5% AND LACTATED RINGER'S IN PLASTIC CONTAINER (CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE)
20MG/100ML;5GM/100ML;328MG/100ML;600MG/100ML;310MG/100ML
Marketing Status: Prescription

Active Ingredient: CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE
Proprietary Name: POTASSIUM CHLORIDE 20MEQ IN DEXTROSE 5% AND LACTATED RINGER'S IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 20MG/100ML;5GM/100ML;328MG/100ML;600MG/100ML;310MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: N019367
Product Number: 005
Approval Date: Apr 5, 1985
Applicant Holder Full Name: BAXTER HEALTHCARE CORP
Marketing Status:  Prescription
Patent and Exclusivity Information

POTASSIUM CHLORIDE 30MEQ IN DEXTROSE 5% AND LACTATED RINGER'S IN PLASTIC CONTAINER (CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE)
20MG/100ML;5GM/100ML;254MG/100ML;600MG/100ML;310MG/100ML
Marketing Status: Prescription

Active Ingredient: CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE
Proprietary Name: POTASSIUM CHLORIDE 30MEQ IN DEXTROSE 5% AND LACTATED RINGER'S IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 20MG/100ML;5GM/100ML;254MG/100ML;600MG/100ML;310MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: N019367
Product Number: 007
Approval Date: Apr 5, 1985
Applicant Holder Full Name: BAXTER HEALTHCARE CORP
Marketing Status:  Prescription
Patent and Exclusivity Information

POTASSIUM CHLORIDE 40MEQ IN DEXTROSE 5% AND LACTATED RINGER'S IN PLASTIC CONTAINER (CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE)
20MG/100ML;5GM/100ML;328MG/100ML;600MG/100ML;310MG/100ML
Marketing Status: Prescription

Active Ingredient: CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE
Proprietary Name: POTASSIUM CHLORIDE 40MEQ IN DEXTROSE 5% AND LACTATED RINGER'S IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 20MG/100ML;5GM/100ML;328MG/100ML;600MG/100ML;310MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: N019367
Product Number: 008
Approval Date: Apr 5, 1985
Applicant Holder Full Name: BAXTER HEALTHCARE CORP
Marketing Status:  Prescription
Patent and Exclusivity Information

POTASSIUM CHLORIDE 5MEQ IN DEXTROSE 5% AND LACTATED RINGER'S IN PLASTIC CONTAINER (CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE)
20MG/100ML;5GM/100ML;105MG/100ML;600MG/100ML;310MG/100ML
Marketing Status: Prescription

Active Ingredient: CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE
Proprietary Name: POTASSIUM CHLORIDE 5MEQ IN DEXTROSE 5% AND LACTATED RINGER'S IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 20MG/100ML;5GM/100ML;105MG/100ML;600MG/100ML;310MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N019367
Product Number: 001
Approval Date: Apr 5, 1985
Applicant Holder Full Name: BAXTER HEALTHCARE CORP
Marketing Status:  Prescription
Patent and Exclusivity Information