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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 020161

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POTASSIUM CHLORIDE 10MEQ IN PLASTIC CONTAINER (POTASSIUM CHLORIDE)
14.9MG/ML
Marketing Status: Prescription
Active Ingredient: POTASSIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE 10MEQ IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 14.9MG/ML
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AP
Application Number: N020161
Product Number: 005
Approval Date: Nov 30, 1992
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status:  Prescription
Patent and Exclusivity Information
POTASSIUM CHLORIDE 10MEQ IN PLASTIC CONTAINER (POTASSIUM CHLORIDE)
745MG/100ML
Marketing Status: Prescription
Active Ingredient: POTASSIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE 10MEQ IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 745MG/100ML
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AP
Application Number: N020161
Product Number: 001
Approval Date: Nov 30, 1992
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status:  Prescription
Patent and Exclusivity Information
POTASSIUM CHLORIDE 20MEQ IN PLASTIC CONTAINER (POTASSIUM CHLORIDE)
29.8MG/ML
Marketing Status: Prescription
Active Ingredient: POTASSIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE 20MEQ IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 29.8MG/ML
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AP
Application Number: N020161
Product Number: 006
Approval Date: Aug 11, 1998
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status:  Prescription
Patent and Exclusivity Information
POTASSIUM CHLORIDE 20MEQ IN PLASTIC CONTAINER (POTASSIUM CHLORIDE)
1.49GM/100ML
Marketing Status: Prescription
Active Ingredient: POTASSIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE 20MEQ IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 1.49GM/100ML
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AP
Application Number: N020161
Product Number: 002
Approval Date: Nov 30, 1992
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status:  Prescription
Patent and Exclusivity Information
POTASSIUM CHLORIDE 40MEQ IN PLASTIC CONTAINER (POTASSIUM CHLORIDE)
2.98GM/100ML
Marketing Status: Prescription
Active Ingredient: POTASSIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE 40MEQ IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 2.98GM/100ML
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AP
Application Number: N020161
Product Number: 004
Approval Date: Aug 11, 1998
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status:  Prescription
Patent and Exclusivity Information
POTASSIUM CHLORIDE 30MEQ IN PLASTIC CONTAINER (POTASSIUM CHLORIDE)
2.24GM/100ML
Marketing Status: Discontinued
Active Ingredient: POTASSIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE 30MEQ IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 2.24GM/100ML
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N020161
Product Number: 003
Approval Date: Aug 11, 1998
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
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