NDC codes

FDA NDC Directory
Product NDC (as listed)11822-4258Labeler and product segments. Claims need a package NDC.
Product NDC at billing width11822-4258Add 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
11822-4258-111822425801118224258011 BOTTLE in 1 CARTON (11822-4258-1) / 20 CAPSULE in 1 BOTTLEMarketed from Jun 24, 2022
11822-4258-211822425802118224258021 BOTTLE in 1 CARTON (11822-4258-2) / 40 CAPSULE in 1 BOTTLEMarketed from Jun 24, 2022
11822-4258-311822425803118224258031 BOTTLE in 1 CARTON (11822-4258-3) / 80 CAPSULE in 1 BOTTLEMarketed from Jun 24, 2022
11822-4258-41182242580411822425804160 CAPSULE in 1 BOTTLE (11822-4258-4)Marketed from Jun 24, 2022
11822-4258-51182242580511822425805300 CAPSULE in 1 BOTTLE (11822-4258-5)Marketed from Jun 24, 2022
11822-4258-61182242580611822425806200 CAPSULE in 1 BOTTLE, PLASTIC (11822-4258-6)Marketed from Apr 12, 2023

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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
Capsule
Route
Oral
Labeler
RITE AID CORPORATIONNDC labeler code 11822
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 207753
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 11822-4258_cf674005-a266-40ec-86eb-8195d1f3ebceSPL ID cf674005-a266-40ec-86eb-8195d1f3ebceSPL set ID de158883-1175-18fc-e053-2995a90a3c96RxCUI 310964UNII WK2XYI10QMUPC 0011822420310

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

N411822425801 followed by a unit qualifier and the quantity

Package 11822-4258-01. 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 the common cold minor pain of arthritis temporarily reduces fever

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 11822-4258

What is NDC 11822-4258?
11822-4258 is the product NDC for Ibuprofen, Ibuprofen 200 mg/1 capsule, listed with the FDA by RITE AID CORPORATION. It has 6 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?
RITE AID CORPORATION, NDC labeler code 11822. 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 207753

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

FDA NDC Directory listings under ANDA 207753
ProductStrengthForm · routeLabelerProduct NDC
IbuprofenIbuprofen 200 mg/1CapsuleOralBetter Living Brands LLC21130-032
IbuprofenIbuprofen 200 mg/1Capsule, Liquid filledOralDolgencorp, Inc. (DOLLAR GENERAL & REXALL)55910-046
IbuprofenIbuprofen 200 mg/1CapsuleOralAurohealth LLC58602-843
IbuprofenIbuprofen 200 mg/1CapsuleOralAurohealth LLC58602-852
IbuprofenIbuprofen 200 mg/1CapsuleOralAurohealth LLC58602-879
IbuprofenIbuprofen 200 mg/1CapsuleOralAurohealth LLC58602-902
IbuprofenIbuprofen 200 mg/1Capsule, Liquid filledOralP & L Development, LLC59726-046

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