Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

Home | Back to Search Results

Product Details for NDA 019218

Expand all

SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER (SODIUM CHLORIDE)
90MG/10ML (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: 90MG/10ML (9MG/ML)
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N019218
Product Number: 001
Approval Date: Jul 13, 1984
Applicant Holder Full Name: ABBOTT LABORATORIES HOSP PRODUCTS DIV
Marketing Status:  Discontinued
Patent and Exclusivity Information

SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER (SODIUM CHLORIDE)
180MG/20ML (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: 180MG/20ML (9MG/ML)
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N019218
Product Number: 002
Approval Date: Apr 30, 1985
Applicant Holder Full Name: ABBOTT LABORATORIES HOSP PRODUCTS DIV
Marketing Status:  Discontinued
Patent and Exclusivity Information