NDC codes

FDA NDC Directory
Product NDC (as listed)68071-5134Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68071-5134Add 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
68071-5134-668071513406680715134066 TABLET, FILM COATED in 1 BOTTLE (68071-5134-6)Marketed from Dec 13, 2019

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 — 400 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
NuCare Pharmaceuticals,Inc.NDC labeler code 68071
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 090796
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 68071-5134_1b54998d-88e6-357a-e063-6394a90a5948SPL ID 1b54998d-88e6-357a-e063-6394a90a5948SPL set ID 999aa615-72b2-9296-e053-2a95a90ac70bRxCUI 197805UNII WK2XYI10QMUPC 0368071513462

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

N468071513406 followed by a unit qualifier and the quantity

Package 68071-5134-06. 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 .

Full label on DailyMed (opens in a new tab)

About NDC 68071-5134

What is NDC 68071-5134?
68071-5134 is the product NDC for Ibuprofen, Ibuprofen 400 mg/1 tablet, film coated, listed with the FDA by NuCare Pharmaceuticals,Inc.. 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?
NuCare Pharmaceuticals,Inc., NDC labeler code 68071. 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 090796

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

FDA NDC Directory listings under ANDA 090796
ProductStrengthForm · routeLabelerProduct NDC
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralDIRECT RX72189-231
IbuprofenIbuprofen 800 mg/1TabletOralMARKSANS PHARMA LIMITED25000-123
IbuprofenIbuprofen 600 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-0426
IbuprofenIbuprofen 400 mg/1TabletOralMARKSANS PHARMA LIMITED25000-121
IbuprofenIbuprofen 600 mg/1TabletOralMARKSANS PHARMA LIMITED25000-122
ibuprofenIbuprofen 400 mg/1TabletOralSKYA HEALTH, LLC73086-210
IbuprofenIbuprofen 800 mg/1Tablet, Film coatedOralDIRECT RX72189-266
ibuprofenIbuprofen 600 mg/1TabletOralSKYA HEALTH, LLC73086-211
IbuprofenIbuprofen 800 mg/1Tablet, Film coatedOralSt. Mary's Medical Park Pharmacy60760-604
ibuprofenIbuprofen 800 mg/1TabletOralSKYA HEALTH, LLC73086-212
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-474
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-4459
IbuprofenIbuprofen 400 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-5126
IbuprofenIbuprofen 800 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-5135
IbuprofenIbuprofen 800 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-5140
IbuprofenIbuprofen 400 mg/1Tablet, Film coatedOralDirect Rx72189-324
IbuprofenIbuprofen 800 mg/1Tablet, Film coatedOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0243
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralQPharma, Inc.42708-097
IbuprofenIbuprofen 800 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-1396
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-3313

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