NDC codes

FDA NDC Directory
Product NDC (as listed)72260-129Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72260-0129Add 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
72260-129-017226001290172260012901250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72260-129-01)Marketed from Jun 30, 2026
72260-129-02722600129027226001290260 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72260-129-02)Marketed from Jun 30, 2026
72260-129-1672260012916722600129161 BLISTER PACK in 1 CARTON (72260-129-16) / 6 TABLET, FILM COATED in 1 BLISTER PACKMarketed from Oct 9, 2026 · Sample package

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)
Combogesic
Generic name (nonproprietary)
acetaminophen and ibuprofen
Active ingredients
Acetaminophen — 325 mg/1Ibuprofen — 97.5 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
AFT Pharmaceuticals US, Inc.NDC labeler code 72260
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 209471
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 72260-129_a986b143-6085-48bb-b0a6-b95f3c1644cdSPL ID a986b143-6085-48bb-b0a6-b95f3c1644cd

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

N472260012901 followed by a unit qualifier and the quantity

Package 72260-0129-01. 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 72260-129

What is NDC 72260-129?
72260-129 is the product NDC for Combogesic, Acetaminophen 325 mg/1; Ibuprofen 97.5 mg/1 tablet, film coated, listed with the FDA by AFT Pharmaceuticals US, Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Combogesic (ACETAMINOPHEN and IBUPROFEN).
What is the active ingredient?
Acetaminophen, Ibuprofen.
Who is the labeler?
AFT Pharmaceuticals US, Inc., NDC labeler code 72260. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Combogesic?
4 other product NDCs are listed under this name. See all Combogesic 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 Combogesic NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Combogesicacetaminophen and ibuprofenAcetaminophen 325 mg/1; Ibuprofen 97.5 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-418168788-4181-01
Combogesicacetaminophen and ibuprofenAcetaminophen 325 mg/1; Ibuprofen 97.5 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-400968788-4009-01
Combogesicacetaminophen and ibuprofenAcetaminophen 325 mg/1; Ibuprofen 97.5 mg/1Tablet, Film coatedOralHikma Pharmaceuticals USA Inc0143-943200143-9432-27
Combogesicacetaminophen and ibuprofenAcetaminophen 325 mg/1; Ibuprofen 97.5 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-316171335-3161-0171335-3161-0371335-3161-04

Other NDCs under NDA 209471

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

FDA NDC Directory listings under NDA 209471
ProductStrengthForm · routeLabelerProduct NDC
Combogesicacetaminophen and ibuprofenAcetaminophen 325 mg/1; Ibuprofen 97.5 mg/1Tablet, Film coatedOralHikma Pharmaceuticals USA Inc0143-9432
Combogesicacetaminophen and ibuprofenAcetaminophen 325 mg/1; Ibuprofen 97.5 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-4009
Combogesicacetaminophen and ibuprofenAcetaminophen 325 mg/1; Ibuprofen 97.5 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-4181
Combogesicacetaminophen and ibuprofenAcetaminophen 325 mg/1; Ibuprofen 97.5 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-3161

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