United States · FDA National Drug Code directory
Diluent
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 49281-912_619c17f6-1c56-4821-9ce4-cfdd5d381d86
- Product NDC
- 49281-912
- Form
- INJECTION
- Composition / generic term
- Sodium Chloride
- Labeler
- Sanofi Vaccines US Inc.
- Marketing category
- BLA
- Marketing start / end (source format)
- 19530522
- Source listing expiry
- 20271231
Source-listed ingredients
- SODIUM CHLORIDE — 4.5 mg/.5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 5 VIAL, SINGLE-DOSE in 1 PACKAGE (49281-912-05) / .6 mL in 1 VIAL, SINGLE-DOSE (49281-912-59) · 49281-912-05
- 1 VIAL, MULTI-DOSE in 1 PACKAGE (49281-912-10) / 3 mL in 1 VIAL, MULTI-DOSE (49281-912-69) · 49281-912-10
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →