What is NDC 80425-0232?

80425-0232 is the product NDC for DoubleDex Kit kit, listed with the FDA by Advanced Rx Pharmacy of Tennessee, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

DoubleDex Kit (Dexamethasone Sodium Phosphate, Povidine Iodine).

Advanced Rx Pharmacy of Tennessee, LLC, NDC labeler code 80425. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for DoubleDex Kit?

1 other product NDC are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

DoubleDex Kit NDC 80425-0232 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)80425-0232Labeler and product segments. Claims need a package NDC.

Product NDC at billing width80425-0232Add 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
80425-0232-1	8042502320180425023201	1 KIT in 1 CARTON (80425-0232-1) * .9 mL in 1 PACKET (67777-419-02) * 5 mL in 1 POUCH * 25 VIAL in 1 TRAY (63323-506-01) / 1 mL in 1 VIALMarketed from May 12, 2023

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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): DoubleDex Kit
Generic name (nonproprietary): dexamethasone sodium phosphate, povidine iodine
Dosage form: Kit
Route: Intramuscular, Intravenous, Topical
Labeler: Advanced Rx Pharmacy of Tennessee, LLCNDC labeler code 80425
Product type: Prescription drug
Marketing category: Unapproved drug (other)
Marketing start: May 12, 2023
Listing expires: Dec 31, 2026
Identifiers: Product ID 80425-0232_2a9b1617-60d2-f8ce-e063-6294a90ab02cSPL ID 2a9b1617-60d2-f8ce-e063-6294a90ab02cSPL set ID fb85dd2c-6c90-6249-e053-6294a90a09faRxCUI 797544, 797730, 1812079

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

N480425023201 followed by a unit qualifier and the quantity

Package 80425-0232-01. 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 Dec 31, 2024.

Indications (excerpt from the label)

INDICATIONS AND USAGE By intravenous or intramuscular injection when oral therapy is not feasible: 1. Endocrine Disorders Primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the drug of choice; synthetic analogs may be used in conjunction with mineralocorticoids where applicable; in infancy, mineralocorticoid supplementation is of particular importance). Acute adrenocortical insufficiency (hydrocortisone or cortisone is the drug of choice; mineralocorticoid supplementation may be necessary, particularly when synthetic analogs are used). Preoperatively, and in the event of serious trauma or illness, in patients with known adrenal insufficiency or when adrenocorti…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 80425-0232

What is NDC 80425-0232?: 80425-0232 is the product NDC for DoubleDex Kit kit, listed with the FDA by Advanced Rx Pharmacy of Tennessee, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: DoubleDex Kit (Dexamethasone Sodium Phosphate, Povidine Iodine).
Who is the labeler?: Advanced Rx Pharmacy of Tennessee, LLC, NDC labeler code 80425. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for DoubleDex Kit?: 1 other product NDC are listed under this name. See all DoubleDex Kit 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 DoubleDex Kit NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
DoubleDex Kitdexamethasone sodium phosphate, povidine iodine	—	KitIntramuscular, Intravenous, Topical	Asclemed USA, Inc.	76420-766	76420-0766-01