NDC codes

FDA NDC Directory
Product NDC (as listed)55910-830Labeler and product segments. Claims need a package NDC.
Product NDC at billing width55910-0830Add 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
55910-830-125591008301255910083012120 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (55910-830-12)Marketed from Mar 16, 2022
55910-830-2055910083020559100830201 BOTTLE, PLASTIC in 1 BOX (55910-830-20) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTICMarketed from Mar 16, 2022
55910-830-215591008302155910083021200 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (55910-830-21)Marketed from Mar 16, 2022
55910-830-4055910083040559100830401 BOTTLE, PLASTIC in 1 BOX (55910-830-40) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTICMarketed from Mar 16, 2022
55910-830-8055910083080559100830801 BOTTLE, PLASTIC in 1 BOX (55910-830-80) / 80 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTICMarketed from Mar 16, 2022

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
Capsule, Liquid filled
Route
Oral
Labeler
Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)NDC labeler code 55910
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 202300
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 55910-830_f1afb906-0fa9-4441-84f6-f4b34944dc3cSPL ID f1afb906-0fa9-4441-84f6-f4b34944dc3cSPL set ID 7d544d8e-fa76-461f-9417-5f1873912eacRxCUI 310964UNII WK2XYI10QMUPC 0359726745406

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

N455910083012 followed by a unit qualifier and the quantity

Package 55910-0830-12. 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 the common cold muscular aches 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 55910-830

What is NDC 55910-830?
55910-830 is the product NDC for Ibuprofen, Ibuprofen 200 mg/1 capsule, liquid filled, listed with the FDA by Dolgencorp, Inc. (DOLLAR GENERAL & REXALL). It has 5 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?
Dolgencorp, Inc. (DOLLAR GENERAL & REXALL), NDC labeler code 55910. 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 202300

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

FDA NDC Directory listings under ANDA 202300
ProductStrengthForm · routeLabelerProduct NDC
IbuprofenIbuprofen 200 mg/1Capsule, Liquid filledOralP & L Development, LLC59726-123
Ibuprofen Pain Reliever/Fever ReduceribuprofenIbuprofen 200 mg/1Capsule, Liquid filledOralAmneal Pharmaceuticals LLC65162-356
Ibuprofen Pain Reliever/Fever ReduceribuprofenIbuprofen 200 mg/1Capsule, Liquid filledOralAmneal Pharmaceuticals LLC65162-770

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