NDC codes

FDA NDC Directory
Product NDC (as listed)83324-149Labeler and product segments. Claims need a package NDC.
Product NDC at billing width83324-0149Add 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
83324-149-36833240149361 BOTTLE in 1 CARTON (83324-149-36) / 36 TABLET, FILM COATED in 1 BOTTLEMarketed from Oct 3, 2024

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 reliever
Generic name (nonproprietary)
acetaminophen and ibuprofen
Active ingredients
Ibuprofen — 125 mg/1Acetaminophen — 250 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 216999
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 83324-149_2397603c-8d88-2e65-e063-6394a90ab73eSPL ID 2397603c-8d88-2e65-e063-6394a90ab73eSPL set ID 2397603c-8d87-2e65-e063-6394a90ab73eRxCUI 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

N483324014936 followed by a unit qualifier and the quantity

Package 83324-0149-36. 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 216999

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

FDA NDC Directory listings under ANDA 216999
ProductStrengthForm · routeLabelerProduct NDC
Acetaminophen and IbuprofenIbuprofen 125 mg/1; Acetaminophen 250 mg/1Tablet, Film coatedOralAMERISOURCE BERGEN46122-742
Acetaminophen and IbuprofenIbuprofen 125 mg/1; Acetaminophen 250 mg/1Tablet, Film coatedOralBionpharma Inc.69452-394
dual action pain relieveracetaminophen and ibuprofenIbuprofen 125 mg/1; Acetaminophen 250 mg/1Tablet, Film coatedOralBionpharma Inc.69452-447
Acetaminophen and IbuprofenIbuprofen 125 mg/1; Acetaminophen 250 mg/1Tablet, Film coatedOralBIONPHARMA INC.69452-469
Acetaminophen and IbuprofenIbuprofen 125 mg/1; Acetaminophen 250 mg/1Tablet, Film coatedOralDISCOUNT DRUG MART, INC.53943-034
Acetaminophen and IbuprofenIbuprofen 125 mg/1; Acetaminophen 250 mg/1Tablet, Film coatedOralAMERISOURCE BERGEN46122-818
Acetaminophen and IbuprofenIbuprofen 125 mg/1; Acetaminophen 250 mg/1Tablet, Film coatedOralCVS Pharmacy51316-955
Acetaminophen and IbuprofenIbuprofen 125 mg/1; Acetaminophen 250 mg/1Tablet, Film coatedOralWALGREEN COMPANY0363-4081
Acetaminophen and IbuprofenIbuprofen 125 mg/1; Acetaminophen 250 mg/1Tablet, Film coatedOralMeijer Distribution Inc79481-6501
dual action pain relieveracetaminophen and ibuprofenIbuprofen 125 mg/1; Acetaminophen 250 mg/1Tablet, Film coatedOralBionpharma Inc.69452-446
dual action pain relieveracetaminophen and ibuprofenIbuprofen 125 mg/1; Acetaminophen 250 mg/1Tablet, Film coatedOralCHAIN DRUG MARKETING ASSOCIATION INC.83324-178

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