Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 018502

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

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: No
Reference Standard: No
TE Code: 
Application Number: N018502
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: MILES LABORATORIES INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

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

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: No
Reference Standard: No
TE Code: 
Application Number: N018502
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: MILES LABORATORIES INC
Marketing Status:  Discontinued
Patent and Exclusivity Information