Product Details for NDA 018371
POTASSIUM CHLORIDE 20MEQ IN DEXTROSE 5% IN PLASTIC CONTAINER (DEXTROSE; POTASSIUM CHLORIDE)
5GM/100ML;149MG/100ML
Marketing Status: Prescription
5GM/100ML;224MG/100ML
Marketing Status: Discontinued
5GM/100ML;298MG/100ML
Marketing Status: Discontinued
5GM/100ML;149MG/100ML
Marketing Status: Prescription
Active Ingredient: DEXTROSE; POTASSIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE 20MEQ IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;149MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N018371
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status: Prescription
Patent and Exclusivity Information
POTASSIUM CHLORIDE 30MEQ IN DEXTROSE 5% IN PLASTIC CONTAINER (DEXTROSE; POTASSIUM CHLORIDE)
Proprietary Name: POTASSIUM CHLORIDE 20MEQ IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;149MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N018371
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status: Prescription
Patent and Exclusivity Information
5GM/100ML;224MG/100ML
Marketing Status: Discontinued
Active Ingredient: DEXTROSE; POTASSIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE 30MEQ IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;224MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N018371
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status: Discontinued
Patent and Exclusivity Information
POTASSIUM CHLORIDE 40MEQ IN DEXTROSE 5% IN PLASTIC CONTAINER (DEXTROSE; POTASSIUM CHLORIDE)
Proprietary Name: POTASSIUM CHLORIDE 30MEQ IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;224MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N018371
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status: Discontinued
Patent and Exclusivity Information
5GM/100ML;298MG/100ML
Marketing Status: Discontinued
Active Ingredient: DEXTROSE; POTASSIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE 40MEQ IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;298MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N018371
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: POTASSIUM CHLORIDE 40MEQ IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;298MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N018371
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status: Discontinued
Patent and Exclusivity Information