What is NDC 0002-6885?

0002-6885 is the product NDC for Baricitinib, Baricitinib 4 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.

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 Baricitinib?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Baricitinib NDC 0002-6885 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)0002-6885Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00002-6885Add 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
0002-6885-30	0000268853000002688530	30 TABLET, FILM COATED in 1 BOTTLE (0002-6885-30)Marketed from Dec 20, 2021

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): Baricitinib
Generic name (nonproprietary): baricitinib
Active ingredients: Baricitinib — 4 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Eli Lilly and CompanyNDC labeler code 0002
Product type: Prescription drug
Marketing category: Emergency use authorization
Marketing start: Dec 20, 2021
Listing expires: Dec 31, 2026
Other FDA classes: Janus Kinase Inhibitors (Mechanism)
Identifiers: Product ID 0002-6885_14a2ffe3-1d7e-4d1b-ac44-1698d5f92da4SPL ID 14a2ffe3-1d7e-4d1b-ac44-1698d5f92da4SPL set ID 7052c055-fedf-453b-86bc-01f5465eb157RxCUI 2588561UNII ISP4442I3Y
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

N400002688530 followed by a unit qualifier and the quantity

Package 00002-6885-30. 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

Current FDA label (SPL), effective May 10, 2022.

Full label on DailyMed (opens in a new tab)

About NDC 0002-6885

What is NDC 0002-6885?: 0002-6885 is the product NDC for Baricitinib, Baricitinib 4 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?: 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 Baricitinib?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.