What is NDC 0264-5802?

0264-5802 is the product NDC for Sodium Chloride, Sodium chloride .9 g/100mL injection, solution, listed with the FDA by B. Braun Medical Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.

B. Braun Medical Inc., NDC labeler code 0264. 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?

116 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 0264-5802 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)0264-5802Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00264-5802Add 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	Copy
0264-5802-00	0026458020000264580200	12 CONTAINER in 1 CASE (0264-5802-00) / 1000 mL in 1 CONTAINERMarketed from Jan 26, 2022
0264-5802-10	0026458021000264580210	24 CONTAINER in 1 CASE (0264-5802-10) / 500 mL in 1 CONTAINERMarketed from Jan 26, 2022

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 g/100mL
Dosage form: Injection, Solution
Route: Intravenous
Labeler: B. Braun Medical Inc.NDC labeler code 0264
Product type: Prescription drug
Marketing category: NDA — New Drug ApplicationApplication NDA 019635
Marketing start: Mar 9, 1998
Listing expires: Dec 31, 2026
Other FDA classes: Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)
Identifiers: Product ID 0264-5802_d34ea9bc-a1f9-402a-97cf-894505cee75dSPL ID d34ea9bc-a1f9-402a-97cf-894505cee75dSPL set ID e44c41ae-c9c8-4dd8-ba6c-cebb585378aaRxCUI 1807552, 1807634, 1807639UNII 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.

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

N400264580200 followed by a unit qualifier and the quantity

Package 00264-5802-00. 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 31, 2022.

Indications (excerpt from the label)

INDICATIONS AND USAGE These intravenous solutions are indicated for use in adults and pediatric patients as sources of electrolytes and water for hydration. 0.9% Sodium Chloride Injection USP is indicated for extracellular fluid replacement, treatment of metabolic alkalosis in the presence of fluid loss and mild sodium depletion. 0.9% Sodium Chloride Injection USP is also indicated for use as a priming solution in hemodialysis procedures and may be used to initiate and terminate blood transfusions without hemolyzing red blood cells. 0.45% Sodium Chloride Injection USP is primarily a hydrating solution and may be used to assess the status of the kidneys, since more water is provided than is r…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0264-5802

What is NDC 0264-5802?: 0264-5802 is the product NDC for Sodium Chloride, Sodium chloride .9 g/100mL injection, solution, listed with the FDA by B. Braun Medical Inc.. It has 2 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?: B. Braun Medical Inc., NDC labeler code 0264. 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?: 116 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 117 Sodium Chloride NDCs

Other NDCs under NDA 019635

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

FDA NDC Directory listings under NDA 019635
Product	Strength	Form · route	Labeler	Product NDC
Sodium Chloride	Sodium chloride .45 g/100mL	Injection, SolutionIntravenous	B. Braun Medical Inc.	0264-5804
Sodium Chloride	Sodium chloride .9 g/100mL	Injection, SolutionIntravenous	B. Braun Medical Inc.	0264-7800
Sodium Chloride	Sodium chloride .45 g/100mL	Injection, SolutionIntravenous	B. Braun Medical Inc.	0264-7802
Sodium Chloride	Sodium chloride 3 g/100mL	Injection, SolutionIntravenous	B. Braun Medical Inc.	0264-7805
Sodium Chloride	Sodium chloride 5 g/100mL	Injection, SolutionIntravenous	B. Braun Medical Inc.	0264-7806
Sodium Chloride	Sodium chloride 9 mg/mL	InjectionIntravenous	B. Braun Medical Inc.	0264-9375