Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 018876

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POTASSIUM CHLORIDE 10MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.3% IN PLASTIC CONTAINER (DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE)
5GM/100ML;74.5MG/100ML;300MG/100ML
Marketing Status: Discontinued

Active Ingredient: DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE 10MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.3% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;74.5MG/100ML;300MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018876
Product Number: 001
Approval Date: Jan 17, 1986
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

POTASSIUM CHLORIDE 10MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.3% IN PLASTIC CONTAINER (DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE)
5GM/100ML;149MG/100ML;300MG/100ML
Marketing Status: Discontinued

Active Ingredient: DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE 10MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.3% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;149MG/100ML;300MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018876
Product Number: 006
Approval Date: Mar 28, 1988
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

POTASSIUM CHLORIDE 15MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.3% IN PLASTIC CONTAINER (DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE)
5GM/100ML;224MG/100ML;300MG/100ML
Marketing Status: Discontinued

Active Ingredient: DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE 15MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.3% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;224MG/100ML;300MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018876
Product Number: 007
Approval Date: Mar 28, 1988
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

POTASSIUM CHLORIDE 20MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.3% IN PLASTIC CONTAINER (DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE)
5GM/100ML;298MG/100ML;300MG/100ML
Marketing Status: Discontinued

Active Ingredient: DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE 20MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.3% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;298MG/100ML;300MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018876
Product Number: 008
Approval Date: Mar 28, 1988
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

POTASSIUM CHLORIDE 20MEQ IN DEXTROSE 5% IN SODIUM CHLORIDE 0.3% IN PLASTIC CONTAINER (DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE)
5GM/100ML;149MG/100ML;300MG/100ML
Marketing Status: Discontinued

Active Ingredient: DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE 20MEQ IN DEXTROSE 5% IN SODIUM CHLORIDE 0.3% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;149MG/100ML;300MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018876
Product Number: 002
Approval Date: Jan 17, 1986
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

POTASSIUM CHLORIDE 30MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.3% IN PLASTIC CONTAINER (DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE)
5GM/100ML;224MG/100ML;300MG/100ML
Marketing Status: Discontinued

Active Ingredient: DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE 30MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.3% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;224MG/100ML;300MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018876
Product Number: 003
Approval Date: Jan 17, 1986
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

POTASSIUM CHLORIDE 40MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.3% IN PLASTIC CONTAINER (DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE)
5GM/100ML;298MG/100ML;300MG/100ML
Marketing Status: Discontinued

Active Ingredient: DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE 40MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.3% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;298MG/100ML;300MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018876
Product Number: 004
Approval Date: Mar 28, 1988
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

POTASSIUM CHLORIDE 5MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.3% IN PLASTIC CONTAINER (DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE)
5GM/100ML;74.5MG/100ML;300MG/100ML
Marketing Status: Discontinued

Active Ingredient: DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE 5MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.3% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;74.5MG/100ML;300MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018876
Product Number: 005
Approval Date: Mar 28, 1988
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

POTASSIUM CHLORIDE 5MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.3% IN PLASTIC CONTAINER (DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE)
5GM/100ML;149MG/100ML;300MG/100ML
Marketing Status: Discontinued

Active Ingredient: DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE 5MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.3% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;149MG/100ML;300MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018876
Product Number: 009
Approval Date: Mar 28, 1988
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status:  Discontinued
Patent and Exclusivity Information