NDC codes

FDA NDC Directory
Product NDC (as listed)11822-7893Labeler and product segments. Claims need a package NDC.
Product NDC at billing width11822-7893Add 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
11822-7893-2118227893021182278930250 TABLET, COATED in 1 BOTTLE (11822-7893-2)Marketed from Jun 1, 2020
11822-7893-51182278930511822789305100 TABLET, COATED in 1 BOTTLE (11822-7893-5)Marketed from Jun 1, 2020

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
Tablet, Coated
Route
Oral
Labeler
RITE AIDNDC labeler code 11822
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 091237
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 11822-7893_d4aaf07c-ae80-1fb3-e053-2a95a90a3f89SPL ID d4aaf07c-ae80-1fb3-e053-2a95a90a3f89SPL set ID a7abf95e-d444-42da-e053-2995a90a88d3RxCUI 310965UNII WK2XYI10QMUPC 0011822789240, 0011822789233

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

N411822789302 followed by a unit qualifier and the quantity

Package 11822-7893-02. 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: backache headache menstrual cramps minor pain of arthritis muscular aches the common cold toothache temporarily reduces fever

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 11822-7893

What is NDC 11822-7893?
11822-7893 is the product NDC for Ibuprofen, Ibuprofen 200 mg/1 tablet, coated, listed with the FDA by RITE AID. It has 2 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, 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 091237

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

FDA NDC Directory listings under ANDA 091237
ProductStrengthForm · routeLabelerProduct NDC
IbuprofenIbuprofen 200 mg/1TabletOralWALGREENS0363-9611
IbuprofenIbuprofen 200 mg/1TabletOralWALGREENS0363-9612
IbuprofenIbuprofen 200 mg/1Tablet, CoatedOralTARGET CORPORATION11673-993
IbuprofenIbuprofen 200 mg/1Tablet, CoatedOralRITE AID11822-8925
Ibuprofenibuprofen tablets usp, 200mgIbuprofen 200 mg/1TabletOralBETTER LIVING BRANDS, LLC21130-992
IbuprofenIbuprofen 200 mg/1TabletOralMARKSANS PHARMA LIMITED25000-135
IbuprofenIbuprofen 200 mg/1TabletOralMARKSANS PHARMA LIMITED25000-136
Ibuprofenibuprofen tablets usp, 200mgIbuprofen 200 mg/1TabletOralKROGER COMPANY41226-612
IbuprofenIbuprofen 200 mg/1Tablet, Film coatedOralTIME CAP LABORATORIES,INC49483-611
IbuprofenIbuprofen 200 mg/1Tablet, Film coatedOralTIME CAP LABORATORIES,INC49483-612
IbuprofenIbuprofen 200 mg/1Tablet, CoatedOralCVS Pharmacy.Inc.69842-489
IbuprofenIbuprofen 200 mg/1TabletOralCVS Pharmacy. Inc.69842-493
IbuprofenIbuprofen 200 mg/1TabletOralCARDINAL HEALTH70000-0597

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