NDC codes

FDA NDC Directory
Product NDC (as listed)72789-363Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72789-0363Add 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
72789-363-017278903630172789036301100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-363-01)Marketed from Nov 27, 2023
72789-363-10727890363107278903631010 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-363-10)Marketed from Nov 7, 2023
72789-363-15727890363157278903631515 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-363-15)Marketed from Nov 28, 2023
72789-363-20727890363207278903632020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-363-20)Marketed from Nov 14, 2023
72789-363-21727890363217278903632121 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-363-21)Marketed from Dec 27, 2023
72789-363-24727890363247278903632424 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-363-24)Marketed from Nov 7, 2023
72789-363-30727890363307278903633030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-363-30)Marketed from Nov 13, 2023
72789-363-40727890363407278903634040 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-363-40)Marketed from Nov 28, 2023
72789-363-60727890363607278903636060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-363-60)Marketed from Nov 17, 2023
72789-363-90727890363907278903639090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-363-90)Marketed from Feb 21, 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 — 600 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
PD-Rx Pharmaceuticals, Inc.NDC labeler code 72789
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 091625
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 72789-363_5720414f-1e90-f6ef-e063-6394a90a98fbSPL ID 5720414f-1e90-f6ef-e063-6394a90a98fbSPL set ID d3a7ebef-f7ab-4b34-b62e-278a8deabf78RxCUI 197806UNII WK2XYI10QMUPC 0372789363301

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

N472789036301 followed by a unit qualifier and the quantity

Package 72789-0363-01. 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 . 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. 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 72789-363

What is NDC 72789-363?
72789-363 is the product NDC for Ibuprofen, Ibuprofen 600 mg/1 tablet, film coated, listed with the FDA by PD-Rx Pharmaceuticals, Inc.. It has 10 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?
PD-Rx Pharmaceuticals, Inc., NDC labeler code 72789. 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?
673 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 600 mg/1Tablet, Film coatedOralMedcore LLC82461-72482461-0724-90
IbuprofenIbuprofen 800 mg/1Tablet, Film coatedOralMedcore LLC82461-72582461-0725-90
IbuprofenIbuprofen 200 mg/1TabletOralAurohealth LLC58602-91358602-0913-1758602-0913-40
IbuprofenIbuprofen 400 mg/1Tablet, Film coatedOralAscend Laboratories, LLC67877-73767877-0737-0167877-0737-0567877-0737-33+1 more
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralAscend Laboratories, LLC67877-73867877-0738-0167877-0738-0567877-0738-30+3 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 674 Ibuprofen NDCs

Other NDCs under ANDA 091625

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

FDA NDC Directory listings under ANDA 091625
ProductStrengthForm · routeLabelerProduct NDC
IbuprofenIbuprofen 400 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-3007
IbuprofenIbuprofen 800 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC82868-069
IbuprofenIbuprofen 800 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.72789-364
IbuprofenIbuprofen 800 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-385
IbuprofenIbuprofen 800 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-0176
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-222
IbuprofenIbuprofen 800 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.72789-382
IbuprofenIbuprofen 400 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-0690
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-1218
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0154
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralUnit Dose Solutions, Inc.87441-044
IbuprofenIbuprofen 400 mg/1Tablet, Film coatedOralProficient Rx LP63187-967
IbuprofenIbuprofen 400 mg/1Tablet, Film coatedOralGranules Pharmaceuticals Inc.70010-066
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralGranules Pharmaceuticals Inc.70010-067
IbuprofenIbuprofen 800 mg/1Tablet, Film coatedOralGranules Pharmaceuticals Inc.70010-068
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralProficient Rx LP63187-980
IbuprofenIbuprofen 800 mg/1Tablet, Film coatedOralProficient Rx LP63187-992
IbuprofenIbuprofen 400 mg/1Tablet, Film coatedOralAscend Laboratories, LLC67877-319
IbuprofenIbuprofen 400 mg/1Tablet, Film coatedOralGranules India Limited62207-354
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralGranules India Limited62207-355

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