What is NDC 63187-527?

63187-527 is the product NDC for Ibuprofen, Ibuprofen 600 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 7 package NDCs, shown above in 10- and 11-digit form.

Proficient Rx LP, NDC labeler code 63187. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Ibuprofen?

674 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Ibuprofen NDC 63187-527 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)63187-527Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63187-0527Add 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
63187-527-20	6318705272063187052720	20 TABLET in 1 BOTTLE (63187-527-20)Marketed from Sep 1, 2016
63187-527-30	6318705273063187052730	30 TABLET in 1 BOTTLE (63187-527-30)Marketed from Aug 3, 2015
63187-527-40	6318705274063187052740	40 TABLET in 1 BOTTLE (63187-527-40)Marketed from Aug 3, 2015
63187-527-45	6318705274563187052745	45 TABLET in 1 BOTTLE (63187-527-45)Marketed from Aug 3, 2015
63187-527-60	6318705276063187052760	60 TABLET in 1 BOTTLE (63187-527-60)Marketed from Aug 3, 2015
63187-527-72	6318705277263187052772	120 TABLET in 1 BOTTLE (63187-527-72)Marketed from Aug 3, 2015
63187-527-90	6318705279063187052790	90 TABLET in 1 BOTTLE (63187-527-90)Marketed from Aug 3, 2015

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 — 600 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Proficient Rx LPNDC labeler code 63187
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078558
Marketing start: Nov 23, 2009
Listing expires: Dec 31, 2027
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 63187-527_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

N463187052720 followed by a unit qualifier and the quantity

Package 63187-0527-20. 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)

About NDC 63187-527

What is NDC 63187-527?: 63187-527 is the product NDC for Ibuprofen, Ibuprofen 600 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 7 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Ibuprofen.
What is the active ingredient?: Ibuprofen.
Who is the labeler?: Proficient Rx LP, NDC labeler code 63187. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Ibuprofen?: 674 other product NDCs are listed under this name. See all Ibuprofen NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Ibuprofen NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Ibuprofen	Ibuprofen 600 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4784	70518-4784-0070518-4784-01
Ibuprofen	Ibuprofen 400 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4786	70518-4786-00
Ibuprofen	Ibuprofen 200 mg/1	TabletOral	Famora Inc	87509-0004	87509-0004-05
Ibuprofen	Ibuprofen 800 mg/1	Tablet, Film coatedOral	Medcore LLC	82461-725	82461-0725-90
Ibuprofen	Ibuprofen 600 mg/1	Tablet, Film coatedOral	Medcore LLC	82461-724	82461-0724-90
Ibuprofen	Ibuprofen 200 mg/1	TabletOral	Aurohealth LLC	58602-913	58602-0913-1758602-0913-40
Ibuprofen	Ibuprofen 600 mg/1	Tablet, Film coatedOral	Ascend Laboratories, LLC	67877-738	67877-0738-0167877-0738-0567877-0738-30+3 more
Ibuprofen	Ibuprofen 400 mg/1	Tablet, Film coatedOral	Ascend Laboratories, LLC	67877-737	67877-0737-0167877-0737-0567877-0737-33+1 more
Ibuprofen	Ibuprofen 800 mg/1	Tablet, Film coatedOral	Ascend Laboratories, LLC	67877-739	67877-0739-0167877-0739-0567877-0739-30+4 more
Ibuprofen	Ibuprofen 200 mg/1	Capsule, Liquid filledOral	GOODSENSE	50804-185	50804-0185-0150804-0185-02

All 675 Ibuprofen NDCs

Other NDCs under ANDA 078558

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

FDA NDC Directory listings under ANDA 078558
Product	Strength	Form · route	Labeler	Product NDC
Ibuprofen	Ibuprofen 800 mg/1	TabletOral	A-S Medication Solutions	50090-6616
Ibuprofen	Ibuprofen 400 mg/1	TabletOral	Amneal Pharmaceuticals of New York LLC	53746-464
Ibuprofen	Ibuprofen 600 mg/1	TabletOral	Amneal Pharmaceuticals of New York LLC	53746-465
Ibuprofen	Ibuprofen 800 mg/1	TabletOral	Amneal Pharmaceuticals of New York LLC	53746-466
Ibuprofen	Ibuprofen 400 mg/1	TabletOral	Cardinal Health 107, LLC	55154-2583
Ibuprofen	Ibuprofen 400 mg/1	TabletOral	American Health Packaging	60687-446
Ibuprofen	Ibuprofen 600 mg/1	TabletOral	American Health Packaging	60687-457
Ibuprofen	Ibuprofen 800 mg/1	TabletOral	American Health Packaging	60687-468
Ibuprofen	Ibuprofen 800 mg/1	TabletOral	Proficient Rx LP	63187-022
Ibuprofen	Ibuprofen 400 mg/1	TabletOral	Proficient Rx LP	63187-489
Ibuprofen	Ibuprofen 800 mg/1	TabletOral	Proficient Rx LP	63187-962
Ibuprofen	Ibuprofen 800 mg/1	TabletOral	Bryant Ranch Prepack	63629-1470
Ibuprofen	Ibuprofen 400 mg/1	TabletOral	Amneal Pharmaceuticals LLC	65162-464
Ibuprofen	Ibuprofen 600 mg/1	TabletOral	Amneal Pharmaceuticals LLC	65162-465
Ibuprofen	Ibuprofen 800 mg/1	TabletOral	Amneal Pharmaceuticals LLC	65162-466
Ibuprofen	Ibuprofen 800 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-3415
Ibuprofen	Ibuprofen 800 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-898
Ibuprofen	Ibuprofen 800 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0047
Ibuprofen	Ibuprofen 400 mg/1	TabletOral	Boswell Pharmacy Services LLC d/b/a BPS Wholesale	83209-464
Ibuprofen	Ibuprofen 800 mg/1	TabletOral	PHOENIX RX LLC	85509-1466