What is NDC 70069-048?

70069-048 is the product NDC for Sodium acetate anhydrous, Sodium acetate anhydrous 164 mg/mL solution, concentrate, listed with the FDA by Somerset Therapeutics, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Somerset Therapeutics, LLC, NDC labeler code 70069. 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 acetate anhydrous?

1 other product NDC are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Sodium acetate anhydrous NDC 70069-048

NDC codes

FDA NDC Directory

Product NDC (as listed)70069-048Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70069-0048Add 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
70069-048-20	7006900482070069004820	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, LLCNDC labeler code 70069
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 219826
Marketing start: Oct 23, 2025
Listing expires: Dec 31, 2026
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.

How CPT relates to drug billing

NDC on a medical claim

N470069004820 followed by a unit qualifier and the quantity

Package 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 Oct 21, 2025. 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.

Full label on DailyMed (opens in a new tab)

About NDC 70069-048

What is NDC 70069-048?: 70069-048 is the product NDC for Sodium acetate anhydrous, Sodium acetate anhydrous 164 mg/mL solution, concentrate, listed with the FDA by Somerset Therapeutics, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Sodium acetate anhydrous.
What is the active ingredient?: Sodium acetate anhydrous.
Who is the labeler?: Somerset Therapeutics, LLC, NDC labeler code 70069. 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 acetate anhydrous?: 1 other product NDC are listed under this name. See all Sodium acetate anhydrous 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 acetate anhydrous NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Sodium acetate anhydrous	Sodium acetate anhydrous 164 mg/mL	Solution, ConcentrateIntravenous	Somerset Therapeutics, LLC	70069-047	70069-0047-25

Other NDCs under ANDA 219826

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

FDA NDC Directory listings under ANDA 219826
Product	Strength	Form · route	Labeler	Product NDC
Sodium acetate anhydrous	Sodium acetate anhydrous 164 mg/mL	Solution, ConcentrateIntravenous	Somerset Therapeutics, LLC	70069-047