What is NDC 0517-6502?

0517-6502 is the product NDC for Selenious Acid, Selenium 6 ug/mL injection, solution, listed with the FDA by American Regent, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

American Regent, Inc., NDC labeler code 0517. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Selenious Acid?

4 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Selenious Acid NDC 0517-6502 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)0517-6502Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00517-6502Add 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
0517-6502-10	0051765021000517650210	10 VIAL, SINGLE-DOSE in 1 BOX (0517-6502-10) / 2 mL in 1 VIAL, SINGLE-DOSE (0517-6502-01)Marketed from Mar 28, 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): Selenious Acid
Generic name (nonproprietary): selenious acid
Active ingredients: Selenium — 6 ug/mL
Dosage form: Injection, Solution
Route: Intravenous
Labeler: American Regent, Inc.NDC labeler code 0517
Product type: Prescription drug
Marketing category: NDA — New Drug ApplicationApplication NDA 209379
Marketing start: Mar 28, 2022
Listing expires: Dec 31, 2026
Identifiers: Product ID 0517-6502_4f6657ea-8dfd-4a74-8a36-9855ca7fd34aSPL ID 4f6657ea-8dfd-4a74-8a36-9855ca7fd34aSPL set ID 49324999-50e3-43ed-a8dd-156d6dbedd9fRxCUI 2176324, 2591522UNII H6241UJ22BUPC 0305176502106

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

N400517650210 followed by a unit qualifier and the quantity

Package 00517-6502-10. 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 Aug 1, 2021.

Indications (excerpt from the label)

Selenious Acid Injection is indicated in adult and pediatric patients as a source of selenium for parenteral nutrition when oral or enteral nutrition is not possible, insufficient, or contraindicated. Selenious Acid Injectionis a trace element indicated in adult and pediatric patients as a source of selenium for parenteral nutrition when oral or enteral nutrition is not possible, insufficient, or contraindicated. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0517-6502

What is NDC 0517-6502?: 0517-6502 is the product NDC for Selenious Acid, Selenium 6 ug/mL injection, solution, listed with the FDA by American Regent, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Selenious Acid.
What is the active ingredient?: Selenium.
Who is the labeler?: American Regent, Inc., NDC labeler code 0517. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Selenious Acid?: 4 other product NDCs are listed under this name. See all Selenious Acid 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 Selenious Acid NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Selenious acid	Selenious acid 40 ug/mL	Injection, SolutionIntravenous	Resor Labs	87944-001	87944-0001-01
Selenious Acid	Selenium 60 ug/mL	Injection, SolutionIntravenous	Gland Pharma Limited	68083-660	68083-0660-05
Selenious Acid	Selenium 40 ug/mL	Injection, SolutionIntravenous	Pangea Pharmaceuticals, LLC	81279-106	81279-0106-05
Selenious Acid	Selenium 60 ug/mL	Injection, SolutionIntravenous	American Regent, Inc.	0517-6560	00517-6560-05

Other NDCs under NDA 209379

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

FDA NDC Directory listings under NDA 209379
Product	Strength	Form · route	Labeler	Product NDC
Selenious Acid	Selenium 60 ug/mL	Injection, SolutionIntravenous	American Regent, Inc.	0517-6560