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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 018744

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POTASSIUM CHLORIDE 0.075% IN DEXTROSE 5% IN PLASTIC CONTAINER (DEXTROSE; POTASSIUM CHLORIDE)
5GM/100ML;75MG/100ML
Marketing Status: Discontinued
Active Ingredient: DEXTROSE; POTASSIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE 0.075% IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;75MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018744
Product Number: 001
Approval Date: Nov 9, 1982
Applicant Holder Full Name: B BRAUN MEDICAL INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
POTASSIUM CHLORIDE 0.15% IN DEXTROSE 5% IN PLASTIC CONTAINER (DEXTROSE; POTASSIUM CHLORIDE)
5GM/100ML;150MG/100ML
Marketing Status: Discontinued
Active Ingredient: DEXTROSE; POTASSIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE 0.15% IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;150MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018744
Product Number: 002
Approval Date: Nov 9, 1982
Applicant Holder Full Name: B BRAUN MEDICAL INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
POTASSIUM CHLORIDE 0.22% IN DEXTROSE 5% IN PLASTIC CONTAINER (DEXTROSE; POTASSIUM CHLORIDE)
5GM/100ML;220MG/100ML
Marketing Status: Discontinued
Active Ingredient: DEXTROSE; POTASSIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE 0.22% IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;220MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018744
Product Number: 003
Approval Date: Nov 9, 1982
Applicant Holder Full Name: B BRAUN MEDICAL INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
POTASSIUM CHLORIDE 0.3% IN DEXTROSE 5% IN PLASTIC CONTAINER (DEXTROSE; POTASSIUM CHLORIDE)
5GM/100ML;300MG/100ML
Marketing Status: Discontinued
Active Ingredient: DEXTROSE; POTASSIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE 0.3% IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;300MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018744
Product Number: 004
Approval Date: Nov 9, 1982
Applicant Holder Full Name: B BRAUN MEDICAL INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
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