NDC codes

FDA NDC Directory
Product NDC (as listed)21130-992Labeler and product segments. Claims need a package NDC.
Product NDC at billing width21130-0992Add 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
21130-992-0121130099201211300992011 BOTTLE in 1 CARTON (21130-992-01) / 100 TABLET in 1 BOTTLEMarketed from Aug 8, 2023
21130-992-0521130099205211300992051 BOTTLE in 1 CARTON (21130-992-05) / 50 TABLET in 1 BOTTLEMarketed from Aug 8, 2023
21130-992-532113009925321130099253500 TABLET in 1 BOTTLE (21130-992-53)Marketed from Aug 8, 2023

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 tablets usp, 200mg
Active ingredients
Ibuprofen — 200 mg/1
Dosage form
Tablet
Route
Oral
Labeler
BETTER LIVING BRANDS, LLCNDC labeler code 21130
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 21130-992_01efeeef-bb93-3c38-e063-6294a90a86bbSPL ID 01efeeef-bb93-3c38-e063-6294a90a86bbSPL set ID eb60a1e5-fb6e-360f-e053-2a95a90ade04RxCUI 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

N421130099201 followed by a unit qualifier and the quantity

Package 21130-0992-01. 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 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 21130-992

What is NDC 21130-992?
21130-992 is the product NDC for Ibuprofen, Ibuprofen 200 mg/1 tablet, listed with the FDA by BETTER LIVING BRANDS, LLC. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Ibuprofen (Ibuprofen Tablets USP, 200mg).
What is the active ingredient?
Ibuprofen.
Who is the labeler?
BETTER LIVING BRANDS, LLC, NDC labeler code 21130. 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 AID11822-7893
IbuprofenIbuprofen 200 mg/1Tablet, CoatedOralRITE AID11822-8925
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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