Ibuprofen NDC 72090-071

NDC codes

FDA NDC Directory

Product NDC (as listed)72090-071Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72090-0071Add 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
72090-071-01	72090007101	500 TABLET in 1 BOTTLE (72090-071-01)Marketed from Jul 29, 2026

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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 — 200 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Pioneer Life Sciences, LLC
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 091355
Marketing start: Jul 29, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 72090-071_17d58272-a7be-4e15-b9e4-e3407a9e8e7fSPL ID 17d58272-a7be-4e15-b9e4-e3407a9e8e7fSPL set ID 291602fa-8ebe-4200-bba7-9798c90f8a50RxCUI 310965UNII WK2XYI10QMUPC 0372090005099
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

N472090007101 followed by a unit qualifier and the quantity

Package 72090-0071-01. 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 Aug 3, 2026.

Indications (excerpt from the label)

Uses ■ temporarily relieves minor aches and pains due to: ■ headache ■ muscular aches ■ minor pain of arthritis ■ toothache ■ backache ■ the common cold ■ menstrual cramps ■temporarily reduces fever

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 091355

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

FDA NDC Directory listings under ANDA 091355
Product	Strength	Form · route	Labeler	Product NDC
Ibuprofen	Ibuprofen 200 mg/1	TabletOral	NUVICARE LLC	84324-039
Ibuprofen Immediate Releaseibuprofen	Ibuprofen 200 mg/1	Tablet, CoatedOral	Strides Pharma Inc	59556-856
Ibuprofen Immediate Releaseibuprofen	Ibuprofen 200 mg/1	Tablet, CoatedOral	Strides Pharma Inc	59556-855