Prescription drug · ANDA
Sodium Chloride NDC 0404-9955
Sodium chloride 9 mg/mL · Injection · Intravenous · Henry Schein, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 0404-9955-10 | 00404995510 | 1 VIAL, SINGLE-DOSE in 1 BAG (0404-9955-10) / 10 mL in 1 VIAL, SINGLE-DOSEMarketed from Jan 12, 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 mg/mL
- Dosage form
- Injection
- Route
- Intravenous
- Labeler
- Henry Schein, Inc.
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 088912
- Marketing start
- Listing expires
- Identifiers
- Product ID 0404-9955_1e6c9f43-8251-45d9-979a-7de12ec9ad32SPL ID 1e6c9f43-8251-45d9-979a-7de12ec9ad32SPL set ID e0466bb3-6c26-4044-b051-69f48b67f632RxCUI 1807637UNII 451W47IQ8X
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.
- NDC on a medical claim
N400404995510followed by a unit qualifier and the quantityPackage 00404-9955-10. 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: This parenteral preparation is indicated only for diluting or dissolving drugs for intravenous, intramuscular, or subcutaneous injection, according to instructions of the manufacturer of the drug to be administered.
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 088912
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Sodium Chloride | Sodium chloride 9 mg/mL | InjectionIntravenous | Fresenius Kabi USA, LLC | 63323-186 |
| Sodium Chloride | Sodium chloride 9 mg/mL | InjectionIntravenous | Cardinal Health 107, LLC | 55154-9357 |