Stibium 20X NDC 48951-8410

NDC codes

FDA NDC Directory

Product NDC (as listed)48951-8410Labeler and product segments. Claims need a package NDC.

Product NDC at billing width48951-8410Add 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
48951-8410-3	48951841003	60 mL in 1 BOTTLE, DROPPER (48951-8410-3)Marketed from Sep 1, 2009

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): Stibium 20X
Generic name (nonproprietary): stibium 20x
Active ingredients: Antimony — 20 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Uriel Pharmacy Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 1, 2009
Listing expires: Dec 31, 2027
Identifiers: Product ID 48951-8410_4e440513-3fe9-ad73-e063-6294a90a0428SPL ID 4e440513-3fe9-ad73-e063-6294a90a0428SPL set ID 13f25caf-51f0-6b2f-e063-6394a90a0920UNII 9IT35J3UV3

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 HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N448951841003 followed by a unit qualifier and the quantity

Package 48951-8410-03. 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

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