NDC codes

FDA NDC Directory
Product NDC (as listed)0074-7094Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00074-7094Add 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 NDC11-digit (billing)PackageCopy
0074-7094-04000747094044 TABLET in 1 BOTTLE (0074-7094-04)Marketed from Oct 6, 2021 · Sample package
0074-7094-300007470943030 TABLET in 1 BOTTLE (0074-7094-30)Marketed from Sep 30, 2021
0074-7094-70000747094704 TABLET in 1 BOTTLE (0074-7094-70)Marketed from Dec 17, 2025 · Sample package

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)
Qulipta
Generic name (nonproprietary)
atogepant
Active ingredients
Atogepant — 60 mg/1
Dosage form
Tablet
Route
Oral
Labeler
AbbVie Inc.NDC labeler code 0074
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 215206
Marketing start
Listing expires
Other FDA classes
Calcitonin Gene-related Peptide Receptor Antagonists (Mechanism)
Identifiers
Product ID 0074-7094_392c0320-ca25-423a-9bc1-d06f6badab07SPL ID 392c0320-ca25-423a-9bc1-d06f6badab07SPL set ID 8c8ab8f4-32bd-497a-befa-70c8a51d8d52RxCUI 2571836, 2571842, 2571844, 2571846, 2571848, 2571850UNII 7CRV8RR151UPC 0300747096305, 0300747094301
Pharmacologic class
Calcitonin Gene-related Peptide Receptor Antagonist

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

N400074709404 followed by a unit qualifier and the quantity

Package 00074-7094-04. 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 .

Indications (excerpt from the label)

QULIPTA is indicated for the preventive treatment of migraine in adults. QULIPTA is a calcitonin gene-related peptide receptor antagonist indicated for the preventive treatment of migraine in adults. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0074-7094

What is NDC 0074-7094?
0074-7094 is the product NDC for Qulipta (atogepant), Atogepant 60 mg/1 tablet, listed with the FDA by AbbVie Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Qulipta (Atogepant).
What is the active ingredient?
Atogepant.
Who is the labeler?
AbbVie Inc., NDC labeler code 0074. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Qulipta?
2 other product NDCs are listed under this name. See all Qulipta 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 Qulipta NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
QuliptaatogepantAtogepant 30 mg/1TabletOralAbbVie Inc.0074-709600074-7096-0400074-7096-3000074-7096-70
QuliptaatogepantAtogepant 10 mg/1TabletOralAbbVie Inc.0074-709500074-7095-30

Other NDCs under NDA 215206

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

FDA NDC Directory listings under NDA 215206
ProductStrengthForm · routeLabelerProduct NDC
QuliptaatogepantAtogepant 30 mg/1TabletOralAbbVie Inc.0074-7096
QuliptaatogepantAtogepant 10 mg/1TabletOralAbbVie Inc.0074-7095

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