What is NDC 0264-7707?

0264-7707 is the product NDC for Isolyte S pH 7.4, Sodium chloride .53 g/100mL + 6 more ingredients 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?

Isolyte S pH 7.4 (SODIUM CHLORIDE, SODIUM GLUCONATE, SODIUM ACETATE, POTASSIUM CHLORIDE, MAGNESIUM CHLORIDE, SODIUM PHOSPHATE, DIBASIC, and POTASSIUM PHOSPHATE).

What is the active ingredient?

Sodium chloride, Sodium gluconate, Sodium acetate, Potassium chloride, Magnesium chloride, Sodium phosphate, Dibasic, Potassium phosphate, Monobasic.

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 Isolyte S pH 7.4?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Isolyte S pH 7.4 NDC 0264-7707 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)0264-7707Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00264-7707Add 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
0264-7707-00	0026477070000264770700	12 CONTAINER in 1 CASE (0264-7707-00) / 1000 mL in 1 CONTAINERMarketed from Sep 29, 1989
0264-7707-10	0026477071000264770710	24 CONTAINER in 1 CASE (0264-7707-10) / 500 mL in 1 CONTAINERMarketed from Sep 29, 1989

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): Isolyte S pH 7.4
Generic name (nonproprietary): sodium chloride, sodium gluconate, sodium acetate, potassium chloride, magnesium chloride, sodium phosphate, dibasic, and potassium phosphate
Active ingredients: Sodium chloride — .53 g/100mLSodium gluconate — .5 g/100mLSodium acetate — .37 g/100mLPotassium chloride — .037 g/100mLMagnesium chloride — .03 g/100mLSodium phosphate, Dibasic — .012 g/100mLPotassium phosphate, Monobasic — .00082 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 019696
Marketing start: Sep 29, 1989
Listing expires: Dec 31, 2026
Other FDA classes: Increased Large Intestinal Motility (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Osmotic Activity (Mechanism)Osmotic Activity (Mechanism)Osmotic Activity (Mechanism)Osmotic Activity (Mechanism)Osmotic Activity (Mechanism)Potassium Compounds (Chemical structure)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 0264-7707_88c0041b-2b08-4ca1-b733-60f8b5723892SPL ID 88c0041b-2b08-4ca1-b733-60f8b5723892SPL set ID 150437b6-320e-4c69-a434-2a26a1f0b2e4RxCUI 800925, 800928UNII 451W47IQ8X, R6Q3791S76, 4550K0SC9B, 660YQ98I10, 02F3473H9O, GR686LBA74, 4J9FJ0HL51
Pharmacologic class: Calculi Dissolution Agent; Osmotic Laxative; Potassium Salt

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

N400264770700 followed by a unit qualifier and the quantity

Package 00264-7707-00. 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 Oct 6, 2023.

Indications (excerpt from the label)

INDICATIONS AND USAGE This solution is indicated for use in adults as a source of electrolytes and water for hydration, and as an alkalinizing agent.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0264-7707

What is NDC 0264-7707?: 0264-7707 is the product NDC for Isolyte S pH 7.4, Sodium chloride .53 g/100mL + 6 more ingredients 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?: Isolyte S pH 7.4 (SODIUM CHLORIDE, SODIUM GLUCONATE, SODIUM ACETATE, POTASSIUM CHLORIDE, MAGNESIUM CHLORIDE, SODIUM PHOSPHATE, DIBASIC, and POTASSIUM PHOSPHATE).
What is the active ingredient?: Sodium chloride, Sodium gluconate, Sodium acetate, Potassium chloride, Magnesium chloride, Sodium phosphate, Dibasic, Potassium phosphate, Monobasic.
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 Isolyte S pH 7.4?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.