Sodium Chloride 51662-1464-01

Package NDC

51662-1464-01

Manufacturer: Hf Acquisition Co Llc, Dba Healthfirst
Dosage Form: Injection, Solution
Route: Intramuscular, Intravenous, And Subcutaneous
Product Type: Human Prescription Drug
Marketing Start: December 12, 2019
Listing Expires: December 31, 2026
Application: NDA018803

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Active Ingredients

Ingredient	Strength
Sodium Chloride	9 mg/mL

Selected Package

51662-1464-01Selected

20 mL in 1 VIAL, SINGLE-DOSE (51662-1464-1)