Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 018030

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DEXTROSE 2.5% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER (DEXTROSE; SODIUM CHLORIDE)
2.5GM/100ML;450MG/100ML
Marketing Status: Discontinued

Active Ingredient: DEXTROSE; SODIUM CHLORIDE
Proprietary Name: DEXTROSE 2.5% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 2.5GM/100ML;450MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018030
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: B BRAUN MEDICAL INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

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

Active Ingredient: DEXTROSE; SODIUM CHLORIDE
Proprietary Name: DEXTROSE 5% AND SODIUM CHLORIDE 0.11% 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: N018030
Product Number: 005
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: B BRAUN MEDICAL INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

DEXTROSE 5% AND SODIUM CHLORIDE 0.2% IN PLASTIC CONTAINER (DEXTROSE; SODIUM CHLORIDE)
5GM/100ML;200MG/100ML
Marketing Status: Discontinued

Active Ingredient: DEXTROSE; SODIUM CHLORIDE
Proprietary Name: DEXTROSE 5% AND SODIUM CHLORIDE 0.2% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;200MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018030
Product Number: 004
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: B BRAUN MEDICAL INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

DEXTROSE 5% AND SODIUM CHLORIDE 0.33% IN PLASTIC CONTAINER (DEXTROSE; SODIUM CHLORIDE)
5GM/100ML;330MG/100ML
Marketing Status: Discontinued

Active Ingredient: DEXTROSE; SODIUM CHLORIDE
Proprietary Name: DEXTROSE 5% AND SODIUM CHLORIDE 0.33% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;330MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018030
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: B BRAUN MEDICAL INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

DEXTROSE 5% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER (DEXTROSE; SODIUM CHLORIDE)
5GM/100ML;450MG/100ML
Marketing Status: Discontinued

Active Ingredient: DEXTROSE; SODIUM CHLORIDE
Proprietary Name: DEXTROSE 5% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;450MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018030
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: B BRAUN MEDICAL INC
Marketing Status:  Discontinued
Patent and Exclusivity Information