Prescription drug · NDA
Olumiant (Baricitinib) NDC 0002-4732
Baricitinib 1 mg/1 · Tablet, Film coated · Oral · Eli Lilly and Company
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 0002-4732-30 | 0000247323000002473230 | 30 TABLET, FILM COATED in 1 BOTTLE (0002-4732-30)Marketed from Oct 8, 2019 |
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)
- Olumiant
- Generic name (nonproprietary)
- baricitinib
- Active ingredients
- Baricitinib — 1 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Eli Lilly and CompanyNDC labeler code 0002
- Product type
- Prescription drug
- Marketing category
- NDA — New Drug ApplicationApplication NDA 207924
- Marketing start
- Listing expires
- Other FDA classes
- Janus Kinase Inhibitors (Mechanism)
- Identifiers
- Product ID 0002-4732_ee836a23-8bb1-4e69-b93b-7ed3558e403dSPL ID ee836a23-8bb1-4e69-b93b-7ed3558e403d
- Pharmacologic class
- Janus Kinase Inhibitor
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
N400002473230followed by a unit qualifier and the quantityPackage 00002-4732-30. 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.
About NDC 0002-4732
- What is NDC 0002-4732?
- 0002-4732 is the product NDC for Olumiant (baricitinib), Baricitinib 1 mg/1 tablet, film coated, listed with the FDA by Eli Lilly and Company. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Olumiant (Baricitinib).
- What is the active ingredient?
- Baricitinib.
- Who is the labeler?
- Eli Lilly and Company, NDC labeler code 0002. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Olumiant?
- 2 other product NDCs are listed under this name. See all Olumiant NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Olumiant products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Olumiantbaricitinib | Baricitinib 4 mg/1 | Tablet, Film coatedOral | Eli Lilly and Company | 0002-4479 | 00002-4479-3000002-4479-61 |
| Olumiantbaricitinib | Baricitinib 2 mg/1 | Tablet, Film coatedOral | Eli Lilly and Company | 0002-4182 | 00002-4182-3000002-4182-61 |
Other NDCs under NDA 207924
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Olumiantbaricitinib | Baricitinib 2 mg/1 | Tablet, Film coatedOral | Eli Lilly and Company | 0002-4182 |
| Olumiantbaricitinib | Baricitinib 4 mg/1 | Tablet, Film coatedOral | Eli Lilly and Company | 0002-4479 |