Active Ingredient: SODIUM CHLORIDE
Proprietary Name: SODIUM CHLORIDE 0.9%
Dosage Form; Route of Administration: SOLUTION; INJECTION
Strength: 90MG/10ML (9MG/ML)
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A206171
Product Number: 002
Approval Date: Jul 21, 2017
Applicant Holder Full Name: SPECTRA MEDICAL DEVICES INC
Marketing Status:
Prescription
Patent and Exclusivity Information