Vaccine · BLA
ActHIB NDC 49281-545
Kit · Sanofi Vaccines US Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 49281-545-03 | 49281054503 | 1 KIT in 1 CARTON (49281-545-03) * .6 mL in 1 VIAL, SINGLE-DOSE (49281-546-58) * .5 mL in 1 VIAL, SINGLE-DOSE (49281-547-58)Marketed from Mar 30, 1993 |
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)
- ActHIB
- Generic name (nonproprietary)
- haemophilus influenzae type b strain 1482 capsular polysaccharide tetanus toxoid conjugate antigen
- Dosage form
- Kit
- Labeler
- Sanofi Vaccines US Inc.
- Product type
- Vaccine
- Marketing category
- BLA — Biologics License ApplicationApplication BLA 103935
- Marketing start
- Listing expires
- Identifiers
- Product ID 49281-545_660dcba7-3301-4330-9492-6800821f129aSPL ID 660dcba7-3301-4330-9492-6800821f129a
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
Immunization administration (CPT 90460–90474)
Giving a vaccine is reported separately from the vaccine product code, with an immunization administration code. Which code applies depends on the patient's age, the route and whether counselling was provided.
- NDC on a medical claim
N449281054503followed by a unit qualifier and the quantityPackage 49281-0545-03. 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
The FDA listing for this product does not reference a label (SPL) set.