NDC codes

FDA NDC Directory
Product NDC (as listed)68071-3696Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68071-3696Add 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
68071-3696-868071369608180 TABLET in 1 BOTTLE (68071-3696-8)Marketed from Oct 8, 2024

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 — 800 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 213794
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 68071-3696_23fafe2b-6563-60a0-e063-6394a90af87aSPL ID 23fafe2b-6563-60a0-e063-6394a90af87aSPL set ID 23fb1113-9f1c-88e0-e063-6394a90a4450RxCUI 197807UNII WK2XYI10QMUPC 0368071369687

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

N468071369608 followed by a unit qualifier and the quantity

Package 68071-3696-08. 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.

Other NDCs under ANDA 213794

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

FDA NDC Directory listings under ANDA 213794
ProductStrengthForm · routeLabelerProduct NDC
IbuprofenIbuprofen 600 mg/1TabletOralNorthStar Rx LLC72603-909
IbuprofenIbuprofen 800 mg/1TabletOralNorthStar Rx LLC72603-910
IbuprofenIbuprofen 600 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-2998
IbuprofenIbuprofen 600 mg/1TabletOralAurobindo Pharma Limited59651-361
IbuprofenIbuprofen 400 mg/1TabletOralAurobindo Pharma Limited59651-360
IbuprofenIbuprofen 800 mg/1TabletOralAurobindo Pharma Limited59651-362
IbuprofenIbuprofen 800 mg/1TabletOralUnit Dose Solutions, Inc.87441-045
IbuprofenIbuprofen 600 mg/1TabletOralA-S Medication Solutions50090-5435
IbuprofenIbuprofen 600 mg/1TabletOralA-S Medication Solutions50090-5433
IbuprofenIbuprofen 800 mg/1TabletOralA-S Medication Solutions50090-5445
IbuprofenIbuprofen 800 mg/1TabletOralA-S Medication Solutions50090-5444
IbuprofenIbuprofen 400 mg/1TabletOralBryant Ranch Prepack71335-2682
IbuprofenIbuprofen 800 mg/1TabletOralA-S Medication Solutions50090-5446
IbuprofenIbuprofen 400 mg/1TabletOralREMEDYREPACK INC.70518-3861
IbuprofenIbuprofen 600 mg/1TabletOralBryant Ranch Prepack71335-2683
IbuprofenIbuprofen 800 mg/1TabletOralBryant Ranch Prepack71335-2689
IbuprofenIbuprofen 800 mg/1TabletOralREMEDYREPACK INC.70518-4010
IbuprofenIbuprofen 800 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-897
IbuprofenIbuprofen 600 mg/1TabletOralREMEDYREPACK INC.70518-4341
IbuprofenIbuprofen 400 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-3442

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