What is NDC 85766-219?

85766-219 is the product NDC for Ibuprofen, Ibuprofen 600 mg/1 tablet, listed with the FDA by Sportpharm LLC. It has 6 package NDCs, shown above in 10- and 11-digit form.

Sportpharm LLC, NDC labeler code 85766. 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?

663 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 85766-219 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)85766-219Labeler and product segments. Claims need a package NDC.

Product NDC at billing width85766-0219Add 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
85766-219-01	85766021901	100 TABLET in 1 BOTTLE (85766-219-01)Marketed from Jun 25, 2026
85766-219-10	85766021910	10 TABLET in 1 BOTTLE (85766-219-10)Marketed from Jun 25, 2026
85766-219-20	85766021920	20 TABLET in 1 BOTTLE (85766-219-20)Marketed from Jun 25, 2026
85766-219-30	85766021930	30 TABLET in 1 BOTTLE (85766-219-30)Marketed from Jun 25, 2026
85766-219-60	85766021960	60 TABLET in 1 BOTTLE (85766-219-60)Marketed from Jun 25, 2026
85766-219-90	85766021990	90 TABLET in 1 BOTTLE (85766-219-90)Marketed from Jun 25, 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 — 600 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Sportpharm LLCNDC labeler code 85766
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 213794
Marketing start: May 8, 2020
Listing expires: Dec 31, 2027
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 85766-219_55249485-3b4a-b59c-e063-6294a90ac229SPL ID 55249485-3b4a-b59c-e063-6294a90ac229SPL set ID cef04ae4-e78a-454d-bb66-84b1d348c106RxCUI 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

N485766021901 followed by a unit qualifier and the quantity

Package 85766-0219-01. 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 Jun 26, 2026. This label includes a boxed warning.

Indications (excerpt from the label)

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

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 85766-219

What is NDC 85766-219?: 85766-219 is the product NDC for Ibuprofen, Ibuprofen 600 mg/1 tablet, listed with the FDA by Sportpharm LLC. It has 6 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?: Sportpharm LLC, NDC labeler code 85766. 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?: 663 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 400 mg/1	Tablet, Film coatedOral	Ascend Laboratories, LLC	67877-737	67877-0737-0167877-0737-0567877-0737-33+1 more
Ibuprofen	Ibuprofen 600 mg/1	Tablet, Film coatedOral	Ascend Laboratories, LLC	67877-738	67877-0738-0167877-0738-0567877-0738-30+3 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
Ibuprofen	Ibuprofen 200 mg/1	Tablet, CoatedOral	Shield Pharmaceuticals Corp	83059-0180	83059-0180-04
Ibuprofen	Ibuprofen 200 mg/1	Capsule, Liquid filledOral	Gobrands, Inc. (Goodnow)	82501-1010	82501-1010-00
Ibuprofen	Ibuprofen 600 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4741	70518-4741-0070518-4741-02
Ibuprofen	Ibuprofen 200 mg/1	Tablet, CoatedOral	P & L Development, LLC	59726-003	59726-0003-50
Ibuprofen	Ibuprofen 200 mg/1	Tablet, Film coatedOral	Amazon.com Services LLC	72288-143	72288-0143-7872288-0143-90
Ibuprofen	Ibuprofen 200 mg/1	TabletOral	NUVICARE LLC	84324-038	84324-0038-01

All 664 Ibuprofen NDCs

Other NDCs under ANDA 213794

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

FDA NDC Directory listings under ANDA 213794
Product	Strength	Form · route	Labeler	Product NDC
Ibuprofen	Ibuprofen 800 mg/1	TabletOral	Proficient Rx LP	82804-293
Ibuprofen	Ibuprofen 800 mg/1	TabletOral	Quality Care Products, LLC	83008-050
Ibuprofen	Ibuprofen 800 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	68071-3696
Ibuprofen	Ibuprofen 400 mg/1	TabletOral	HAWAII REPACK, INC.	85534-0011
Ibuprofen	Ibuprofen 600 mg/1	TabletOral	REMEDYREPACK INC.	70518-4341
Ibuprofen	Ibuprofen 800 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-897
Ibuprofen	Ibuprofen 600 mg/1	TabletOral	HAWAII REPACK, INC.	85534-0012
Ibuprofen	Ibuprofen 800 mg/1	TabletOral	HAWAII REPACK, INC.	85534-0013
Ibuprofen	Ibuprofen 400 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-3442
Ibuprofen	Ibuprofen 800 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8319
Ibuprofen	Ibuprofen 400 mg/1	TabletOral	Asclemed USA, Inc.	76420-575
Ibuprofen	Ibuprofen 600 mg/1	TabletOral	Asclemed USA, Inc.	76420-576
Ibuprofen	Ibuprofen 800 mg/1	TabletOral	Asclemed USA, Inc.	76420-577
Ibuprofen	Ibuprofen 800 mg/1	TabletOral	A-S Medication Solutions	50090-6886
Ibuprofen	Ibuprofen 400 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-3507
Ibuprofen	Ibuprofen 800 mg/1	TabletOral	Direct_Rx	72189-556
Ibuprofen	Ibuprofen 800 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-929
Ibuprofen	Ibuprofen 600 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8354
Ibuprofen	Ibuprofen 600 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0424
Ibuprofen	Ibuprofen 400 mg/1	TabletOral	Direct_rx	72189-564

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