NDC codes

FDA NDC Directory
Product NDC (as listed)42507-909Labeler and product segments. Claims need a package NDC.
Product NDC at billing width42507-0909Add 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
42507-909-224250709092242507090922200 TABLET, COATED in 1 BOTTLE, PLASTIC (42507-909-22)Marketed from Jan 13, 2026

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 — 200 mg/1
Dosage form
Tablet, Coated
Route
Oral
Labeler
HYVEE INCNDC labeler code 42507
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 079174
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 42507-909_484bfcdc-6b80-766b-e063-6294a90a37bbSPL ID 484bfcdc-6b80-766b-e063-6294a90a37bbSPL set ID 45aead8a-37ee-9a66-e063-6394a90a5d17RxCUI 310965UNII 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

N442507090922 followed by a unit qualifier and the quantity

Package 42507-0909-22. 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 muscular aches minor pain of arthritis toothache backache the common cold menstrual cramps temporarily reduces fever

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 42507-909

What is NDC 42507-909?
42507-909 is the product NDC for Ibuprofen, Ibuprofen 200 mg/1 tablet, coated, listed with the FDA by HYVEE INC. It has 1 package NDC, 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?
HYVEE INC, NDC labeler code 42507. 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 079174

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

FDA NDC Directory listings under ANDA 079174
ProductStrengthForm · routeLabelerProduct NDC
IbuprofenIbuprofen 200 mg/1TabletOralTOPCO ASSOCIATES LLC36800-663
Ibuprofen ThompsonibuprofenIbuprofen 200 mg/1Tablet, CoatedOralThompson Safety73408-809
Ibuprofen 200 MgibuprofenIbuprofen 200 mg/1TabletOralBasic Drugs, Inc.0761-0908
IbuprofenIbuprofen 200 mg/1Tablet, CoatedOralGrocery Outlet, Inc.85828-110
Unishield IbuprofenibuprofenIbuprofen 200 mg/1Tablet, CoatedOralUnishield49314-1003
IbuprofenIbuprofen 200 mg/1Tablet, CoatedOralLidl US LLC71141-114
IbuprofenIbuprofen 200 mg/1TabletOralBI-MART37835-585
IbuprofenIbuprofen 200 mg/1TabletOralBi-Mart37835-581
Circle K IbuprofenibuprofenIbuprofen 200 mg/1Tablet, CoatedOralLil Drug Store Products, Inc66715-5507
IbuprofenIbuprofen 200 mg/1Tablet, CoatedOralAAA Pharmaceutical, Inc.57344-309
Ibuprofenibuprofen 200mgIbuprofen 200 mg/1Tablet, Film coatedOralADVANCED FIRST AID, INC.67060-001
IbuprofenIbuprofen 200 mg/1TabletOralGranules India Limited62207-365
IbuprofenIbuprofen 200 mg/1TabletOralGranules India Limited62207-366
McKesson Ibuprofen 200 mgibuprofenIbuprofen 200 mg/1Tablet, CoatedOralMcKesson Medical-Surgical68599-8051
IbuprofenIbuprofen 200 mg/1TabletOralGranules India Limited62207-395
IbuprofenIbuprofen 200 mg/1TabletOralGranules India Limited62207-396
Physicians Care Ibuprofenibuprofen 200mgIbuprofen 200 mg/1Tablet, Film coatedOralAcme United Corporation0924-0076
Ibuprofen, Caseys 4goodibuprofen tabletsIbuprofen 200 mg/1Tablet, Film coatedOralLil' Drug Store Products, Inc.66715-6307
IbuprofenIbuprofen 200 mg/1Tablet, CoatedOralUnited Natural Foods, Inc. dba UNFI41163-509
IbuprofenIbuprofen 200 mg/1TabletOralPuraCap Pharmaceutical LLC51013-319

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