Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 019699

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POTASSIUM CHLORIDE 0.15% IN DEXTROSE 5% IN PLASTIC CONTAINER (DEXTROSE; POTASSIUM CHLORIDE)
5GM/100ML;150MG/100ML
Marketing Status: Prescription

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: AP
Application Number: N019699
Product Number: 004
Approval Date: Sep 29, 1989
Applicant Holder Full Name: B BRAUN MEDICAL INC
Marketing Status:  Prescription
Patent and Exclusivity Information

POTASSIUM CHLORIDE 0.3% IN DEXTROSE 5% IN PLASTIC CONTAINER (DEXTROSE; POTASSIUM CHLORIDE)
5GM/100ML;300MG/100ML
Marketing Status: Prescription

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: AP
Application Number: N019699
Product Number: 006
Approval Date: Sep 29, 1989
Applicant Holder Full Name: B BRAUN MEDICAL INC
Marketing Status:  Prescription
Patent and Exclusivity Information

POTASSIUM CHLORIDE 0.037% IN DEXTROSE 5% IN PLASTIC CONTAINER (DEXTROSE; POTASSIUM CHLORIDE)
5GM/100ML;37MG/100ML
Marketing Status: Discontinued

Active Ingredient: DEXTROSE; POTASSIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE 0.037% IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;37MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N019699
Product Number: 001
Approval Date: Sep 29, 1989
Applicant Holder Full Name: B BRAUN MEDICAL INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

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: N019699
Product Number: 002
Approval Date: Sep 29, 1989
Applicant Holder Full Name: B BRAUN MEDICAL INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

POTASSIUM CHLORIDE 0.11% IN DEXTROSE 5% IN PLASTIC CONTAINER (DEXTROSE; POTASSIUM CHLORIDE)
5GM/100ML;110MG/100ML
Marketing Status: Discontinued

Active Ingredient: DEXTROSE; POTASSIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE 0.11% IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;110MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N019699
Product Number: 003
Approval Date: Sep 29, 1989
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: N019699
Product Number: 005
Approval Date: Sep 29, 1989
Applicant Holder Full Name: B BRAUN MEDICAL INC
Marketing Status:  Discontinued
Patent and Exclusivity Information