Product Details for NDA 019691
POTASSIUM CHLORIDE 20MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER (DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE)
5GM/100ML;149MG/100ML;900MG/100ML
Marketing Status: Prescription
5GM/100ML;298MG/100ML;900MG/100ML
Marketing Status: Prescription
5GM/100ML;74.5MG/100ML;900MG/100ML
Marketing Status: Discontinued
5GM/100ML;149MG/100ML;900MG/100ML
Marketing Status: Discontinued
5GM/100ML;224MG/100ML;900MG/100ML
Marketing Status: Discontinued
5GM/100ML;298MG/100ML;900MG/100ML
Marketing Status: Discontinued
5GM/100ML;224MG/100ML;900MG/100ML
Marketing Status: Discontinued
5GM/100ML;74.5MG/100ML;900MG/100ML
Marketing Status: Discontinued
5GM/100ML;149MG/100ML;900MG/100ML
Marketing Status: Discontinued
5GM/100ML;149MG/100ML;900MG/100ML
Marketing Status: Prescription
Active Ingredient: DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE 20MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;149MG/100ML;900MG/100ML
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AP
Application Number: N019691
Product Number: 005
Approval Date: Mar 24, 1988
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status: Prescription
Patent and Exclusivity Information
POTASSIUM CHLORIDE 40MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER (DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE)
Proprietary Name: POTASSIUM CHLORIDE 20MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;149MG/100ML;900MG/100ML
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AP
Application Number: N019691
Product Number: 005
Approval Date: Mar 24, 1988
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status: Prescription
Patent and Exclusivity Information
5GM/100ML;298MG/100ML;900MG/100ML
Marketing Status: Prescription
Active Ingredient: DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE 40MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;298MG/100ML;900MG/100ML
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AP
Application Number: N019691
Product Number: 009
Approval Date: Mar 24, 1988
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status: Prescription
Patent and Exclusivity Information
POTASSIUM CHLORIDE 10MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER (DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE)
Proprietary Name: POTASSIUM CHLORIDE 40MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;298MG/100ML;900MG/100ML
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AP
Application Number: N019691
Product Number: 009
Approval Date: Mar 24, 1988
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status: Prescription
Patent and Exclusivity Information
5GM/100ML;74.5MG/100ML;900MG/100ML
Marketing Status: Discontinued
Active Ingredient: DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE 10MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;74.5MG/100ML;900MG/100ML
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019691
Product Number: 002
Approval Date: Mar 24, 1988
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status: Discontinued
Patent and Exclusivity Information
POTASSIUM CHLORIDE 10MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER (DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE)
Proprietary Name: POTASSIUM CHLORIDE 10MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;74.5MG/100ML;900MG/100ML
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019691
Product Number: 002
Approval Date: Mar 24, 1988
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status: Discontinued
Patent and Exclusivity Information
5GM/100ML;149MG/100ML;900MG/100ML
Marketing Status: Discontinued
Active Ingredient: DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE 10MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;149MG/100ML;900MG/100ML
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019691
Product Number: 004
Approval Date: Mar 24, 1988
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status: Discontinued
Patent and Exclusivity Information
POTASSIUM CHLORIDE 15MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER (DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE)
Proprietary Name: POTASSIUM CHLORIDE 10MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;149MG/100ML;900MG/100ML
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019691
Product Number: 004
Approval Date: Mar 24, 1988
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status: Discontinued
Patent and Exclusivity Information
5GM/100ML;224MG/100ML;900MG/100ML
Marketing Status: Discontinued
Active Ingredient: DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE 15MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;224MG/100ML;900MG/100ML
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019691
Product Number: 006
Approval Date: Mar 24, 1988
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status: Discontinued
Patent and Exclusivity Information
POTASSIUM CHLORIDE 20MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER (DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE)
Proprietary Name: POTASSIUM CHLORIDE 15MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;224MG/100ML;900MG/100ML
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019691
Product Number: 006
Approval Date: Mar 24, 1988
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status: Discontinued
Patent and Exclusivity Information
5GM/100ML;298MG/100ML;900MG/100ML
Marketing Status: Discontinued
Active Ingredient: DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE 20MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;298MG/100ML;900MG/100ML
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019691
Product Number: 008
Approval Date: Mar 24, 1988
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status: Discontinued
Patent and Exclusivity Information
POTASSIUM CHLORIDE 30MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER (DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE)
Proprietary Name: POTASSIUM CHLORIDE 20MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;298MG/100ML;900MG/100ML
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019691
Product Number: 008
Approval Date: Mar 24, 1988
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status: Discontinued
Patent and Exclusivity Information
5GM/100ML;224MG/100ML;900MG/100ML
Marketing Status: Discontinued
Active Ingredient: DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE 30MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;224MG/100ML;900MG/100ML
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019691
Product Number: 007
Approval Date: Mar 24, 1988
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status: Discontinued
Patent and Exclusivity Information
POTASSIUM CHLORIDE 5MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER (DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE)
Proprietary Name: POTASSIUM CHLORIDE 30MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;224MG/100ML;900MG/100ML
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019691
Product Number: 007
Approval Date: Mar 24, 1988
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status: Discontinued
Patent and Exclusivity Information
5GM/100ML;74.5MG/100ML;900MG/100ML
Marketing Status: Discontinued
Active Ingredient: DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE 5MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;74.5MG/100ML;900MG/100ML
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019691
Product Number: 001
Approval Date: Mar 24, 1988
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status: Discontinued
Patent and Exclusivity Information
POTASSIUM CHLORIDE 5MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER (DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE)
Proprietary Name: POTASSIUM CHLORIDE 5MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;74.5MG/100ML;900MG/100ML
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019691
Product Number: 001
Approval Date: Mar 24, 1988
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status: Discontinued
Patent and Exclusivity Information
5GM/100ML;149MG/100ML;900MG/100ML
Marketing Status: Discontinued
Active Ingredient: DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE 5MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;149MG/100ML;900MG/100ML
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019691
Product Number: 003
Approval Date: Mar 24, 1988
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: POTASSIUM CHLORIDE 5MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;149MG/100ML;900MG/100ML
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019691
Product Number: 003
Approval Date: Mar 24, 1988
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status: Discontinued
Patent and Exclusivity Information