NDC codes

FDA NDC Directory
Product NDC (as listed)0143-9432Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00143-9432Add 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
0143-9432-2700143943227250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0143-9432-27)Marketed from Jan 6, 2025

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)
Combogesic
Generic name (nonproprietary)
acetaminophen and ibuprofen
Active ingredients
Acetaminophen — 325 mg/1Ibuprofen — 97.5 mg/1
Dosage form
Tablet, Film coated
Route
Oral
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 0143-9432_186821ca-5ce7-403e-9470-39f6691cd492SPL ID 186821ca-5ce7-403e-9470-39f6691cd492SPL set ID b32651c4-7fa0-415b-91eb-854aa1c28f2aRxCUI 2675760, 2675765UNII 362O9ITL9D, WK2XYI10QM

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

N400143943227 followed by a unit qualifier and the quantity

Package 00143-9432-27. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

COMBOGESIC is indicated in adults for the short-term management of mild to moderate acute pain. COMBOGESIC is a combination of acetaminophen and ibuprofen, a non-steroidal anti-inflammatory drug (NSAID), and is indicated in adults for the short term management of mild to moderate acute pain ( 1 ).

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

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 coatedOralAFT Pharmaceuticals US, Inc.72260-129
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
Combogesicacetaminophen and ibuprofenAcetaminophen 325 mg/1; Ibuprofen 97.5 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-4009

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