NDC codes

FDA NDC Directory
Product NDC (as listed)68071-4952Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68071-4952Add 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
68071-4952-4680714952046807149520440 TABLET, FILM COATED in 1 BOTTLE (68071-4952-4)Marketed from Jul 2, 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 078329
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 68071-4952_1b2e33e8-26b3-e5a0-e063-6294a90ae585SPL ID 1b2e33e8-26b3-e5a0-e063-6294a90ae585SPL set ID 8cb93e5f-4ebc-24b7-e053-2a95a90a5a23RxCUI 197805UNII WK2XYI10QMUPC 0368071495249

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

N468071495204 followed by a unit qualifier and the quantity

Package 68071-4952-04. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

About NDC 68071-4952

What is NDC 68071-4952?
68071-4952 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?
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 078329

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

FDA NDC Directory listings under ANDA 078329
ProductStrengthForm · routeLabelerProduct NDC
IbuprofenIbuprofen 400 mg/1Tablet, Film coatedOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8309
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8310
IbuprofenIbuprofen 800 mg/1Tablet, Film coatedOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8311
IbuprofenIbuprofen 400 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-5818
IbuprofenIbuprofen 400 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-5819
IbuprofenIbuprofen 800 mg/1Tablet, Film coatedOralSt. Mary's Medical Park Pharmacy60760-596
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralST. MARY'S MEDICAL PARK PHARMACY60760-597
IbuprofenIbuprofen 800 mg/1Tablet, Film coatedOralStrides Pharma Science Limited64380-807
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralStrides Pharma Science Limited64380-808
IbuprofenIbuprofen 400 mg/1Tablet, Film coatedOralStrides Pharma Science Limited64380-809
IbuprofenIbuprofen 800 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-4845
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-4887
IbuprofenIbuprofen 800 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-4949
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-4968
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-5066
IbuprofenIbuprofen 400 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-5228
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-8531
IbuprofenIbuprofen 800 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-8710
IbuprofenIbuprofen 400 mg/1Tablet, Film coatedOralAmneal Pharmaceuticals NY LLC69238-1101
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralAmneal Pharmaceuticals NY LLC69238-1102

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