Acetaminophen 250 mg and Ibuprofen 125 mg NDC 51672-4258

NDC codes

FDA NDC Directory

Product NDC (as listed)51672-4258Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51672-4258Add 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 NDC	11-digit (billing)	Package	Copy
51672-4258-1	51672425801	1 BOTTLE in 1 CARTON (51672-4258-1) / 216 TABLET in 1 BOTTLEMarketed from Mar 15, 2026
51672-4258-4	51672425804	1 BOTTLE in 1 CARTON (51672-4258-4) / 72 TABLET in 1 BOTTLEMarketed from Mar 15, 2026

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): Acetaminophen 250 mg and Ibuprofen 125 mg
Generic name (nonproprietary): acetaminophen 250 mg and ibuprofen 125 mg tablets
Active ingredients: Acetaminophen — 250 mg/1Ibuprofen — 125 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Sun Pharmaceutical Industries, Inc.
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 219053
Marketing start: Mar 15, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 51672-4258_4cb287fd-c316-032c-e063-6294a90a6ffeSPL ID 4cb287fd-c316-032c-e063-6294a90a6ffeSPL set ID 2a31a975-72f9-2a16-e063-6394a90a8149RxCUI 2387532UNII 362O9ITL9D, WK2XYI10QM
Pharmacologic class: Nonsteroidal Anti-inflammatory Drug

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

N451672425801 followed by a unit qualifier and the quantity

Package 51672-4258-01. 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 Mar 10, 2026.

Indications (excerpt from the label)

Uses • temporarily relieves minor aches and pains due to: headache toothache backache menstrual cramps muscular aches minor pain of arthritis

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)