Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 018722

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SODIUM CHLORIDE 0.9% AND POTASSIUM CHLORIDE 0.075% IN PLASTIC CONTAINER (POTASSIUM CHLORIDE; SODIUM CHLORIDE)
75MG/100ML;900MG/100ML
Marketing Status: Discontinued

Active Ingredient: POTASSIUM CHLORIDE; SODIUM CHLORIDE
Proprietary Name: SODIUM CHLORIDE 0.9% AND POTASSIUM CHLORIDE 0.075% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 75MG/100ML;900MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018722
Product Number: 001
Approval Date: Nov 9, 1982
Applicant Holder Full Name: B BRAUN MEDICAL INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

SODIUM CHLORIDE 0.9% AND POTASSIUM CHLORIDE 0.15% IN PLASTIC CONTAINER (POTASSIUM CHLORIDE; SODIUM CHLORIDE)
150MG/100ML;900MG/100ML
Marketing Status: Discontinued

Active Ingredient: POTASSIUM CHLORIDE; SODIUM CHLORIDE
Proprietary Name: SODIUM CHLORIDE 0.9% AND POTASSIUM CHLORIDE 0.15% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 150MG/100ML;900MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018722
Product Number: 002
Approval Date: Nov 9, 1982
Applicant Holder Full Name: B BRAUN MEDICAL INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

SODIUM CHLORIDE 0.9% AND POTASSIUM CHLORIDE 0.22% IN PLASTIC CONTAINER (POTASSIUM CHLORIDE; SODIUM CHLORIDE)
220MG/100ML;900MG/100ML
Marketing Status: Discontinued

Active Ingredient: POTASSIUM CHLORIDE; SODIUM CHLORIDE
Proprietary Name: SODIUM CHLORIDE 0.9% AND POTASSIUM CHLORIDE 0.22% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 220MG/100ML;900MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018722
Product Number: 003
Approval Date: Nov 9, 1982
Applicant Holder Full Name: B BRAUN MEDICAL INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

SODIUM CHLORIDE 0.9% AND POTASSIUM CHLORIDE 0.3% IN PLASTIC CONTAINER (POTASSIUM CHLORIDE; SODIUM CHLORIDE)
300MG/100ML;900MG/100ML
Marketing Status: Discontinued

Active Ingredient: POTASSIUM CHLORIDE; SODIUM CHLORIDE
Proprietary Name: SODIUM CHLORIDE 0.9% AND POTASSIUM CHLORIDE 0.3% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 300MG/100ML;900MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018722
Product Number: 004
Approval Date: Nov 9, 1982
Applicant Holder Full Name: B BRAUN MEDICAL INC
Marketing Status:  Discontinued
Patent and Exclusivity Information