NDC codes

FDA NDC Directory
Product NDC (as listed)11673-924Labeler and product segments. Claims need a package NDC.
Product NDC at billing width11673-0924Add 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
11673-924-75116730924751 BOTTLE in 1 CARTON (11673-924-75) / 72 TABLET in 1 BOTTLEMarketed from Jul 11, 2023

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)
Dual Action Pain Relief
Generic name (nonproprietary)
acetaminophen, ibuprofen
Active ingredients
Ibuprofen — 125 mg/1Acetaminophen — 250 mg/1
Dosage form
Tablet
Route
Oral
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 216994
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 11673-924_22ecfa46-dbe4-249f-e063-6394a90a70afSPL ID 22ecfa46-dbe4-249f-e063-6394a90a70afSPL set ID e680652b-30d8-6009-e053-2995a90abe29RxCUI 2387532UNII WK2XYI10QM, 362O9ITL9D

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

N411673092475 followed by a unit qualifier and the quantity

Package 11673-0924-75. 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)

Uses temporarily relieves minor aches and pains due to: headache toothache backache menstrual cramps muscular aches minor pain of arthritis

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 216994

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

FDA NDC Directory listings under ANDA 216994
ProductStrengthForm · routeLabelerProduct NDC
Dual Actionacetaminophen, ibuprofenAcetaminophen 250 mg/1; Ibuprofen 125 mg/1TabletOralKROGER COMPANY41226-716
Dual Action Pain Reliefacetaminophen, ibuprofenAcetaminophen 250 mg/1; Ibuprofen 125 mg/1TabletOralTIME CAP LABORATORIES, INC.49483-716
Acetaminophen 250 mg and Ibuprofen 125 mgacetaminophen 250 mg and ibuprofen 125 mg tabletsAcetaminophen 250 mg/1; Ibuprofen 125 mg/1Tablet, Film coatedOralMARKSANS PHARMA LIMITED25000-080
Dual Actionacetaminophen, ibuprofenAcetaminophen 250 mg/1; Ibuprofen 125 mg/1TabletOralBETTER LIVING BRANDS, LLC21130-716

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