What is NDC 0487-4301?

0487-4301 is the product NDC for Sodium Chloride, Sodium chloride 9 mg/mL injection, listed with the FDA by Nephron Pharmaceuticals Corporation. It has 4 package NDCs, shown above in 10- and 11-digit form.

Nephron Pharmaceuticals Corporation, NDC labeler code 0487. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Sodium Chloride NDC 0487-4301 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)0487-4301Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00487-4301Add 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 NDC	11-digit (billing)	Package
0487-4301-05	0048743010500487430105	64 BAG in 1 CASE (0487-4301-05) / 50 mL in 1 BAGMarketed from Jun 4, 2020
0487-4301-10	0048743011000487430110	64 BAG in 1 CASE (0487-4301-10) / 100 mL in 1 BAGMarketed from Jun 4, 2020
0487-4301-25	0048743012500487430125	35 BAG in 1 CASE (0487-4301-25) / 250 mL in 1 BAGMarketed from Jun 4, 2020
0487-4301-50	0048743015000487430150	18 BAG in 1 CASE (0487-4301-50) / 500 mL in 1 BAGMarketed from Jun 4, 2020

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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 mg/mL
Dosage form: Injection
Route: Intravenous
Labeler: Nephron Pharmaceuticals CorporationNDC labeler code 0487
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 211968
Marketing start: Jun 4, 2020
Listing expires: Dec 31, 2027
Identifiers: Product ID 0487-4301_49545dc2-5776-da02-e063-6394a90a7ef0SPL ID 49545dc2-5776-da02-e063-6394a90a7ef0SPL set ID a4edf2d5-a9ff-30d4-e053-2995a90a5650RxCUI 1807631, 1807632, 1807633, 1807634UNII 451W47IQ8XUPC 0304874301257, 0000000000000, 0304874301509, 0304874301059, 0304874301103

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.

Administration

Drug administration (CPT 96360–96549)

When a clinician administers the drug, the administration is reported separately. Codes in this range cover hydration, therapeutic injections and infusions, and chemotherapy or other complex drug administration. The right code depends on route, duration and drug type, and self-administered drugs are not billed this way.

How CPT relates to drug billing

NDC on a medical claim

N400487430105 followed by a unit qualifier and the quantity

Package 00487-4301-05. 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 Jan 26, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE Sodium Chloride Injection, USP is indicated as a source of water and electrolytes. 0.9% Sodium Chloride Injection, USP is also indicated for use as a priming solution in hemodialysis procedures.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0487-4301

What is NDC 0487-4301?: 0487-4301 is the product NDC for Sodium Chloride, Sodium chloride 9 mg/mL injection, listed with the FDA by Nephron Pharmaceuticals Corporation. It has 4 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?: Nephron Pharmaceuticals Corporation, NDC labeler code 0487. 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Sodium Chloride	Sodium chloride 50 mg/g	OintmentOphthalmic	YYBA CORP	73581-707	73581-0707-0173581-0707-03
Sodium Chloride	Sodium chloride 1 g/1	TabletOral	Method Pharmaceuticals, LLC	58657-119	58657-0119-01
Sodium chloride	Sodium chloride .9 g/100mL	Injection, SolutionIrrigation	Fresenius Kabi USA, LLC	65219-502	65219-0502-10
Sodium chloride	Sodium chloride .9 g/100mL	Injection, SolutionIrrigation	Fresenius Kabi USA, LLC	65219-504	65219-0504-20
Sodium chloride	Sodium chloride .9 g/100mL	Injection, SolutionIrrigation	Becton Dickinson and Company	17271-800	17271-0800-0717271-0800-0817271-0800-09
Sodium Chloride	Sodium chloride 1000 mg/1	TabletOral	Rising Pharma Holdings, Inc.	57237-361	57237-0361-01
Sodium chloride	Sodium chloride .9 g/100mL	Injection, SolutionIrrigation	Fresenius Kabi USA, LLC	65219-506	65219-0506-30
Sodium Chloridesodium chloride tablets	Sodium chloride 1000 mg/1	TabletOral	Kesin Pharma Corporation	81033-028	81033-0028-01
Sodium Chloridesodium chloride tablet	Sodium chloride 1000 mg/1	TabletOral	Belleview Bioscience LLC	84447-002	84447-0002-01
Sodium Chloride	Sodium chloride 900 mg/100mL	IrrigantIrrigation	Baxter Healthcare Company	0338-9834	00338-9834-04

All 120 Sodium Chloride NDCs