NDC codes

FDA NDC Directory
Product NDC (as listed)10267-3846Labeler and product segments. Claims need a package NDC.
Product NDC at billing width10267-3846Add 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
10267-3846-21026738460210267384602250 TABLET in 1 BOTTLE (10267-3846-2)Marketed from Jan 15, 2014

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
Route
Oral
Labeler
Contract Pharmacal Corp.NDC labeler code 10267
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 071265
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 10267-3846_77cf0092-7436-14ba-e053-2991aa0ac112SPL ID 77cf0092-7436-14ba-e053-2991aa0ac112SPL set ID 237bcb87-64a0-415b-bd53-e9d3b8bf33b6RxCUI 310965UNII WK2XYI10QMUPC 0310267390920, 0310267385223

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

N410267384602 followed by a unit qualifier and the quantity

Package 10267-3846-02. 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: headache muscular ache 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 10267-3846

What is NDC 10267-3846?
10267-3846 is the product NDC for ibuprofen, Ibuprofen 200 mg/1 tablet, listed with the FDA by Contract Pharmacal Corp.. It has 1 package NDC, 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?
Contract Pharmacal Corp., NDC labeler code 10267. 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?
672 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 400 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-480170518-4801-00
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

All 673 ibuprofen NDCs

Other NDCs under ANDA 071265

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

FDA NDC Directory listings under ANDA 071265
ProductStrengthForm · routeLabelerProduct NDC
ibuprofenIbuprofen 200 mg/1TabletOralContract Pharmacal Corp.10267-3852
ibuprofenIbuprofen 200 mg/1TabletOralContract Pharmacal Corp.10267-3909

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