Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 020178

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SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER (SODIUM CHLORIDE)
450MG/50ML (9MG/ML)
Marketing Status: Prescription

Active Ingredient: SODIUM CHLORIDE
Proprietary Name: SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: SOLUTION; INJECTION
Strength: 450MG/50ML (9MG/ML)
Reference Listed Drug: Yes
Reference Standard: No
TE Code: AP
Application Number: N020178
Product Number: 002
Approval Date: Dec 7, 1992
Applicant Holder Full Name: BAXTER HEALTHCARE CORP
Marketing Status:  Prescription
Patent and Exclusivity Information

SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER (SODIUM CHLORIDE)
900MG/100ML
Marketing Status: Prescription

Active Ingredient: SODIUM CHLORIDE
Proprietary Name: SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: SOLUTION; INJECTION
Strength: 900MG/100ML
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AP
Application Number: N020178
Product Number: 001
Approval Date: Dec 7, 1992
Applicant Holder Full Name: BAXTER HEALTHCARE CORP
Marketing Status:  Prescription
Patent and Exclusivity Information