Prescription drug · ANDA
Sodium acetate anhydrous NDC 70069-048
Sodium acetate anhydrous 164 mg/mL · Solution, Concentrate · Intravenous · Somerset Therapeutics, LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70069-048-20 | 70069004820 | 20 VIAL, GLASS in 1 CARTON (70069-048-20) / 100 mL in 1 VIAL, GLASSMarketed from Oct 23, 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 acetate anhydrous
- Generic name (nonproprietary)
- sodium acetate anhydrous
- Active ingredients
- Sodium acetate anhydrous — 164 mg/mL
- Dosage form
- Solution, Concentrate
- Route
- Intravenous
- Labeler
- Somerset Therapeutics, LLC
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 219826
- Marketing start
- Listing expires
- Identifiers
- Product ID 70069-048_1aae3237-9555-442b-b962-619d23f7e00aSPL ID 1aae3237-9555-442b-b962-619d23f7e00aSPL set ID 93edebd6-ef7f-483a-80b6-bfaf34ea5dedRxCUI 237371UNII NVG71ZZ7P0UPC 0370069047255, 0370069048207, 0370069047019, 0370069048016
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
N470069004820followed by a unit qualifier and the quantityPackage 70069-0048-20. 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 . This label includes a boxed warning.
Indications (excerpt from the label)
INDICATIONS AND USAGE Sodium acetate injection (2 mEq/mL) is indicated as a source of sodium for addition to large volume intravenous fluids to prevent or correct hyponatremia in patients with restricted or no oral intake. It is also useful as an additive for preparing specific intravenous fluid formulas when the needs of the patient cannot be met by standard electrolyte or nutrient solutions.
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 219826
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 acetate anhydrous | Sodium acetate anhydrous 164 mg/mL | Solution, ConcentrateIntravenous | Somerset Therapeutics, LLC | 70069-047 |