Ibuprofen NDC 63187-022

NDC codes

FDA NDC Directory

Product NDC (as listed)63187-022Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63187-0022Add 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
63187-022-15	63187002215	15 TABLET in 1 BOTTLE (63187-022-15)Marketed from May 1, 2014
63187-022-20	63187002220	20 TABLET in 1 BOTTLE (63187-022-20)Marketed from Sep 1, 2016
63187-022-21	63187002221	21 TABLET in 1 BOTTLE (63187-022-21)Marketed from Sep 1, 2017
63187-022-30	63187002230	30 TABLET in 1 BOTTLE (63187-022-30)Marketed from May 1, 2014
63187-022-40	63187002240	40 TABLET in 1 BOTTLE (63187-022-40)Marketed from May 1, 2014
63187-022-45	63187002245	45 TABLET in 1 BOTTLE (63187-022-45)Marketed from May 1, 2014
63187-022-60	63187002260	60 TABLET in 1 BOTTLE (63187-022-60)Marketed from May 1, 2014
63187-022-72	63187002272	120 TABLET in 1 BOTTLE (63187-022-72)Marketed from May 1, 2014
63187-022-90	63187002290	90 TABLET in 1 BOTTLE (63187-022-90)Marketed from May 1, 2014

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 — 800 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Proficient Rx LP
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078558
Marketing start: Nov 23, 2009
Listing expires: Dec 31, 2026
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 63187-022_7db62aa5-dd71-4f62-b656-c4df75686f02SPL ID 7db62aa5-dd71-4f62-b656-c4df75686f02SPL set ID e23eb275-ce0c-40ec-b809-a48c5e46c7ecRxCUI 197805, 197806, 197807UNII 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

N463187002215 followed by a unit qualifier and the quantity

Package 63187-0022-15. 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 Jan 1, 2021. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Carefully consider the potential benefits and risks of Ibuprofen Tablets, USP and other treatment options before deciding to use Ibuprofen Tablets, USP. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see WARNINGS ). Ibuprofen Tablets, USP are indicated for relief of the signs and symptoms of rheumatoid arthritis and osteoarthritis. Ibuprofen Tablets, USP are indicated for relief of mild to moderate pain. Ibuprofen Tablets, USP are also indicated for the treatment of primary dysmenorrhea. Controlled clinical trials to establish the safety and effectiveness of Ibuprofen Tablets, USP in children have not been con…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)