NDC codes

FDA NDC Directory
Product NDC (as listed)80425-0243Labeler and product segments. Claims need a package NDC.
Product NDC at billing width80425-0243Add 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
80425-0243-480425024304100 TABLET, FILM COATED in 1 BOTTLE (80425-0243-4)Marketed from Jan 10, 2023

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, Film coated
Route
Oral
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 80425-0243_2a9aec09-630b-2252-e063-6294a90a204aSPL ID 2a9aec09-630b-2252-e063-6294a90a204aSPL set ID f18b6a0a-e42f-083d-e053-2995a90a40e4RxCUI 197807UNII WK2XYI10QM

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

N480425024304 followed by a unit qualifier and the quantity

Package 80425-0243-04. 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.

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 400 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.43063-872
IbuprofenIbuprofen 800 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-5140
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-474
IbuprofenIbuprofen 800 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-1396
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-4459
IbuprofenIbuprofen 400 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-5126
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.43063-867
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-532
IbuprofenIbuprofen 800 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-5135
IbuprofenIbuprofen 400 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-5134
IbuprofenIbuprofen 800 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.43063-914
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-1503
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-3313
IbuprofenIbuprofen 400 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-1517
IbuprofenIbuprofen 400 mg/1TabletOralMARKSANS PHARMA LIMITED25000-121
IbuprofenIbuprofen 600 mg/1TabletOralMARKSANS PHARMA LIMITED25000-122
IbuprofenIbuprofen 800 mg/1TabletOralMARKSANS PHARMA LIMITED25000-123
IbuprofenIbuprofen 400 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-2432
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralDIRECT RX72189-231
ibuprofenIbuprofen 800 mg/1TabletOralSKYA HEALTH, LLC73086-212

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