NDC codes

FDA NDC Directory
Product NDC (as listed)17271-800Labeler and product segments. Claims need a package NDC.
Product NDC at billing width17271-0800Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
17271-800-0717271080007172710800076 BAG in 1 CASE (17271-800-07) / 1000 mL in 1 BAGMarketed from Jan 2, 2026
17271-800-0817271080008172710800085 BAG in 1 CASE (17271-800-08) / 2000 mL in 1 BAGMarketed from Jan 2, 2026
17271-800-0917271080009172710800094 BAG in 1 CASE (17271-800-09) / 3000 mL in 1 BAGMarketed from Nov 14, 2025

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Sodium chloride
Generic name (nonproprietary)
sodium chloride
Active ingredients
Sodium chloride — .9 g/100mL
Dosage form
Injection, Solution
Route
Irrigation
Labeler
Becton Dickinson and CompanyNDC labeler code 17271
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 213688
Marketing start
Listing expires
Other FDA classes
Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)
Identifiers
Product ID 17271-800_ca3355f2-2cf0-4f58-bed5-0c4c0a7d3511SPL ID ca3355f2-2cf0-4f58-bed5-0c4c0a7d3511SPL set ID ca3355f2-2cf0-4f58-bed5-0c4c0a7d3511RxCUI 486515UNII 451W47IQ8X
Pharmacologic class
Osmotic Laxative

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N417271080007 followed by a unit qualifier and the quantity

Package 17271-0800-07. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective .

Indications (excerpt from the label)

INDICATIONS AND USAGE 0.9% Sodium Chloride Irrigation is indicated for all general irrigation, washing, rinsing and dilution purposes which permit use of a sterile, nonpyrogenic electrolyte solution.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 17271-800

What is NDC 17271-800?
17271-800 is the product NDC for Sodium chloride, Sodium chloride .9 g/100mL injection, solution, listed with the FDA by Becton Dickinson and Company. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Sodium chloride.
What is the active ingredient?
Sodium chloride.
Who is the labeler?
Becton Dickinson and Company, NDC labeler code 17271. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Sodium chloride?
119 other product NDCs are listed under this name. See all Sodium chloride NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Sodium chloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Sodium ChlorideSodium chloride 50 mg/gOintmentOphthalmicYYBA CORP73581-70773581-0707-0173581-0707-03
Sodium ChlorideSodium chloride 1 g/1TabletOralMethod Pharmaceuticals, LLC58657-11958657-0119-01
Sodium chlorideSodium chloride .9 g/100mLInjection, SolutionIrrigationFresenius Kabi USA, LLC65219-50265219-0502-10
Sodium chlorideSodium chloride .9 g/100mLInjection, SolutionIrrigationFresenius Kabi USA, LLC65219-50465219-0504-20
Sodium ChlorideSodium chloride 1000 mg/1TabletOralRising Pharma Holdings, Inc.57237-36157237-0361-01
Sodium chlorideSodium chloride .9 g/100mLInjection, SolutionIrrigationFresenius Kabi USA, LLC65219-50665219-0506-30
Sodium Chloridesodium chloride tabletsSodium chloride 1000 mg/1TabletOralKesin Pharma Corporation81033-02881033-0028-01
Sodium Chloridesodium chloride tabletSodium chloride 1000 mg/1TabletOralBelleview Bioscience LLC84447-00284447-0002-01
Sodium ChlorideSodium chloride 900 mg/100mLIrrigantIrrigationBaxter Healthcare Company0338-983400338-9834-04
Sodium ChlorideSodium chloride 900 mg/100mLIrrigantIrrigationBaxter Healthcare Company0338-011000338-0110-04

All 120 Sodium chloride NDCs

Other NDCs under ANDA 213688

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 213688
ProductStrengthForm · routeLabelerProduct NDC
Sodium chlorideSodium chloride .9 g/100mLInjection, SolutionIrrigationFresenius Kabi USA, LLC65219-502
Sodium chlorideSodium chloride .9 g/100mLInjection, SolutionIrrigationFresenius Kabi USA, LLC65219-504
Sodium chlorideSodium chloride .9 g/100mLInjection, SolutionIrrigationFresenius Kabi USA, LLC65219-506

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