Ibuprofen NDC 21130-032

NDC codes

FDA NDC Directory

Product NDC (as listed)21130-032Labeler and product segments. Claims need a package NDC.

Product NDC at billing width21130-0032Add 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
21130-032-12	21130003212	1 BOTTLE in 1 CARTON (21130-032-12) / 40 CAPSULE in 1 BOTTLEMarketed from Sep 20, 2023
21130-032-18	21130003218	1 BOTTLE in 1 CARTON (21130-032-18) / 80 CAPSULE in 1 BOTTLEMarketed from Sep 20, 2023
21130-032-32	21130003232	180 CAPSULE in 1 BOTTLE (21130-032-32)Marketed from Sep 20, 2023
21130-032-38	21130003238	300 CAPSULE in 1 BOTTLE (21130-032-38)Marketed from Sep 20, 2023

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: Capsule
Route: Oral
Labeler: Better Living Brands LLC
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 207753
Marketing start: Sep 20, 2023
Listing expires: Dec 31, 2026
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 21130-032_30a207f5-34a7-45ca-a1f8-5576b71c48d9SPL ID 30a207f5-34a7-45ca-a1f8-5576b71c48d9SPL set ID f6ef7f73-b5ab-4c82-e053-6394a90ac81eRxCUI 310964UNII 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

N421130003212 followed by a unit qualifier and the quantity

Package 21130-0032-12. 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 Sep 22, 2023.

Indications (excerpt from the label)

Uses temporarily relieves minor aches and pains due to: headache toothache backache menstrual cramps muscular aches the common cold minor pain of arthritis 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 207753

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

FDA NDC Directory listings under ANDA 207753
Product	Strength	Form · route	Labeler	Product NDC
Ibuprofen	Ibuprofen 200 mg/1	CapsuleOral	RITE AID CORPORATION	11822-4258
Ibuprofen	Ibuprofen 200 mg/1	Capsule, Liquid filledOral	Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)	55910-046
Ibuprofen	Ibuprofen 200 mg/1	Capsule, Liquid filledOral	P & L Development, LLC	59726-046
Ibuprofen	Ibuprofen 200 mg/1	CapsuleOral	Aurohealth LLC	58602-843
Ibuprofen	Ibuprofen 200 mg/1	CapsuleOral	Aurohealth LLC	58602-852
Ibuprofen	Ibuprofen 200 mg/1	CapsuleOral	Aurohealth LLC	58602-879
Ibuprofen	Ibuprofen 200 mg/1	CapsuleOral	Aurohealth LLC	58602-902