United States · FDA National Drug Code directory
Sodium chloride
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
- 17271-701_31344de2-e115-440a-a913-ff63da5f17d8
- Product NDC
- 17271-701
- Form
- INJECTION, SOLUTION
- Composition / generic term
- SODIUM CHLORIDE
- Labeler
- Becton Dickinson and Company
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170919
- Source listing expiry
- 20261231
Source-listed ingredients
- SODIUM CHLORIDE — 9 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 50 mL in 1 BAG (17271-701-02) · 17271-701-02
- 100 mL in 1 BAG (17271-701-03) · 17271-701-03
- 250 mL in 1 BAG (17271-701-05) · 17271-701-05
- 500 mL in 1 BAG (17271-701-06) · 17271-701-06
- 1000 mL in 1 BAG (17271-701-07) · 17271-701-07
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 →