Product Details for NDA 019367
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
20MG/100ML;5GM/100ML;179MG/100ML;600MG/100ML;310MG/100ML
Marketing Status: Prescription
20MG/100ML;5GM/100ML;254MG/100ML;600MG/100ML;310MG/100ML
Marketing Status: Prescription
20MG/100ML;5GM/100ML;179MG/100ML;600MG/100ML;310MG/100ML
Marketing Status: Prescription
20MG/100ML;5GM/100ML;328MG/100ML;600MG/100ML;310MG/100ML
Marketing Status: Prescription
20MG/100ML;5GM/100ML;254MG/100ML;600MG/100ML;310MG/100ML
Marketing Status: Prescription
20MG/100ML;5GM/100ML;328MG/100ML;600MG/100ML;310MG/100ML
Marketing Status: Prescription
20MG/100ML;5GM/100ML;105MG/100ML;600MG/100ML;310MG/100ML
Marketing Status: Prescription
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)
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
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)
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
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)
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
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)
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
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)
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
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)
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
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)
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
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
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