NDC codes

FDA NDC Directory
Product NDC (as listed)83209-464Labeler and product segments. Claims need a package NDC.
Product NDC at billing width83209-0464Add 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
83209-464-0983209046409832090464099 TABLET in 1 BLISTER PACK (83209-464-09)Marketed from Jun 3, 2024
83209-464-10832090464108320904641010 TABLET in 1 BLISTER PACK (83209-464-10)Marketed from Jun 3, 2024
83209-464-12832090464128320904641212 TABLET in 1 BLISTER PACK (83209-464-12)Marketed from Jun 3, 2024
83209-464-14832090464148320904641414 TABLET in 1 BLISTER PACK (83209-464-14)Marketed from Jun 3, 2024
83209-464-15832090464158320904641515 TABLET in 1 BLISTER PACK (83209-464-15)Marketed from Jun 3, 2024
83209-464-18832090464188320904641818 TABLET in 1 BLISTER PACK (83209-464-18)Marketed from Jun 3, 2024
83209-464-20832090464208320904642020 TABLET in 1 BLISTER PACK (83209-464-20)Marketed from Jun 3, 2024
83209-464-21832090464218320904642121 TABLET in 1 BLISTER PACK (83209-464-21)Marketed from Jun 3, 2024
83209-464-24832090464248320904642424 TABLET in 1 BLISTER PACK (83209-464-24)Marketed from Jun 3, 2024
83209-464-28832090464288320904642828 TABLET in 1 BLISTER PACK (83209-464-28)Marketed from Jun 3, 2024
83209-464-30832090464308320904643030 TABLET in 1 BLISTER PACK (83209-464-30)Marketed from Jun 3, 2024
83209-464-40832090464408320904644040 TABLET in 1 BLISTER PACK (83209-464-40)Marketed from Jun 3, 2024
83209-464-60832090464608320904646060 TABLET in 1 BLISTER PACK (83209-464-60)Marketed from Jun 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)
Ibuprofen
Generic name (nonproprietary)
ibuprofen
Active ingredients
Ibuprofen — 400 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 078558
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 83209-464_1a0301ba-9f66-ac39-e063-6394a90a34bbSPL ID 1a0301ba-9f66-ac39-e063-6394a90a34bbSPL set ID 1a02fa34-b5ae-7183-e063-6294a90a3ae4RxCUI 197805UNII 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

N483209046409 followed by a unit qualifier and the quantity

Package 83209-0464-09. 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)

INDICATIONS AND USAGE Carefully consider the potential benefits and risks of Ibuprofen Tablets and other treatment options before deciding to use Ibuprofen Tablets. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals [see WARNINGS ]. Ibuprofen Tablets are indicated for relief of the signs and symptoms of rheumatoid arthritis and osteoarthritis. Ibuprofen Tablets are indicated for relief of mild to moderate pain. Ibuprofen Tablets are also indicated for the treatment of primary dysmenorrhea. Controlled clinical trials to establish the safety and effectiveness of Ibuprofen Tablets in children have not been conducted.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 83209-464

What is NDC 83209-464?
83209-464 is the product NDC for Ibuprofen, Ibuprofen 400 mg/1 tablet, listed with the FDA by Boswell Pharmacy Services LLC d/b/a BPS Wholesale. It has 13 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Ibuprofen.
What is the active ingredient?
Ibuprofen.
Who is the labeler?
Boswell Pharmacy Services LLC d/b/a BPS Wholesale, NDC labeler code 83209. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Ibuprofen?
674 other product NDCs are listed under this name. See all Ibuprofen 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 Ibuprofen NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-478470518-4784-0070518-4784-01
IbuprofenIbuprofen 400 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-478670518-4786-00
IbuprofenIbuprofen 200 mg/1TabletOralFamora Inc87509-000487509-0004-05
IbuprofenIbuprofen 800 mg/1Tablet, Film coatedOralMedcore LLC82461-72582461-0725-90
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralMedcore LLC82461-72482461-0724-90
IbuprofenIbuprofen 200 mg/1TabletOralAurohealth LLC58602-91358602-0913-1758602-0913-40
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralAscend Laboratories, LLC67877-73867877-0738-0167877-0738-0567877-0738-30+3 more
IbuprofenIbuprofen 400 mg/1Tablet, Film coatedOralAscend Laboratories, LLC67877-73767877-0737-0167877-0737-0567877-0737-33+1 more
IbuprofenIbuprofen 800 mg/1Tablet, Film coatedOralAscend Laboratories, LLC67877-73967877-0739-0167877-0739-0567877-0739-30+4 more
IbuprofenIbuprofen 200 mg/1Capsule, Liquid filledOralGOODSENSE50804-18550804-0185-0150804-0185-02

All 675 Ibuprofen NDCs

Other NDCs under ANDA 078558

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

FDA NDC Directory listings under ANDA 078558
ProductStrengthForm · routeLabelerProduct NDC
IbuprofenIbuprofen 800 mg/1TabletOralA-S Medication Solutions50090-6616
IbuprofenIbuprofen 400 mg/1TabletOralAmneal Pharmaceuticals of New York LLC53746-464
IbuprofenIbuprofen 600 mg/1TabletOralAmneal Pharmaceuticals of New York LLC53746-465
IbuprofenIbuprofen 800 mg/1TabletOralAmneal Pharmaceuticals of New York LLC53746-466
IbuprofenIbuprofen 400 mg/1TabletOralCardinal Health 107, LLC55154-2583
IbuprofenIbuprofen 400 mg/1TabletOralAmerican Health Packaging60687-446
IbuprofenIbuprofen 600 mg/1TabletOralAmerican Health Packaging60687-457
IbuprofenIbuprofen 800 mg/1TabletOralAmerican Health Packaging60687-468
IbuprofenIbuprofen 800 mg/1TabletOralProficient Rx LP63187-022
IbuprofenIbuprofen 400 mg/1TabletOralProficient Rx LP63187-489
IbuprofenIbuprofen 600 mg/1TabletOralProficient Rx LP63187-527
IbuprofenIbuprofen 800 mg/1TabletOralProficient Rx LP63187-962
IbuprofenIbuprofen 800 mg/1TabletOralBryant Ranch Prepack63629-1470
IbuprofenIbuprofen 400 mg/1TabletOralAmneal Pharmaceuticals LLC65162-464
IbuprofenIbuprofen 600 mg/1TabletOralAmneal Pharmaceuticals LLC65162-465
IbuprofenIbuprofen 800 mg/1TabletOralAmneal Pharmaceuticals LLC65162-466
IbuprofenIbuprofen 800 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-3415
IbuprofenIbuprofen 800 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-898
IbuprofenIbuprofen 800 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-0047
IbuprofenIbuprofen 800 mg/1TabletOralPHOENIX RX LLC85509-1466

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