What is NDC 85509-2750?

85509-2750 is the product NDC for Diclofenac Potassium, Diclofenac potassium 50 mg/1 tablet, film coated, listed with the FDA by Phoenix RX LLC. It has 4 package NDCs, shown above in 10- and 11-digit form.

Phoenix RX LLC, NDC labeler code 85509. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Diclofenac Potassium?

67 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Diclofenac Potassium NDC 85509-2750

NDC codes

FDA NDC Directory

Product NDC (as listed)85509-2750Labeler and product segments. Claims need a package NDC.

Product NDC at billing width85509-2750Add 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
85509-2750-1	8550927500185509275001	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (85509-2750-1)Marketed from Nov 5, 2025
85509-2750-3	8550927500385509275003	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (85509-2750-3)Marketed from Oct 29, 2025
85509-2750-6	8550927500685509275006	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (85509-2750-6)Marketed from Oct 29, 2025
85509-2750-9	8550927500985509275009	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (85509-2750-9)Marketed from Oct 29, 2025

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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): Diclofenac Potassium
Generic name (nonproprietary): diclofenac potassium
Active ingredients: Diclofenac potassium — 50 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Phoenix RX LLCNDC labeler code 85509
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 215787
Marketing start: Oct 21, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)Decreased Prostaglandin Production (Physiologic effect)
Identifiers: Product ID 85509-2750_43069d0f-e508-d0c7-e063-6394a90a3e02SPL ID 43069d0f-e508-d0c7-e063-6394a90a3e02SPL set ID 3fd418ac-49f6-d520-e063-6394a90afbd8RxCUI 855942UNII L4D5UA6CB4
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

N485509275001 followed by a unit qualifier and the quantity

Package 85509-2750-01. 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 Nov 7, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Carefully consider the potential benefits and risks of diclofenac potassium tablets and other treatment options before deciding to use diclofenac potassium tablets. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see WARNINGS: Gastrointestinal Bleeding, Ulceration, and Perforation) . Diclofenac potassium tablets are indicated: for treatment of primary dysmenorrhea for relief of mild to moderate pain for relief of the signs and symptoms of osteoarthritis for relief of the signs and symptoms of rheumatoid arthritis

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 85509-2750

What is NDC 85509-2750?: 85509-2750 is the product NDC for Diclofenac Potassium, Diclofenac potassium 50 mg/1 tablet, film coated, listed with the FDA by Phoenix RX LLC. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Diclofenac Potassium.
What is the active ingredient?: Diclofenac potassium.
Who is the labeler?: Phoenix RX LLC, NDC labeler code 85509. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Diclofenac Potassium?: 67 other product NDCs are listed under this name. See all Diclofenac Potassium 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 Diclofenac Potassium NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Diclofenac Potassium	Diclofenac potassium 75 mg/1	Tablet, CoatedOral	Advagen Pharma Ltd	72888-203	72888-0203-0072888-0203-0172888-0203-05+1 more
Diclofenac Potassiumdiclofenac potassium, film coated	Diclofenac potassium 50 mg/1	TabletOral	Amerisyn LLC	87564-011	87564-0011-10
Diclofenac Potassiumdiclofenac potassium, film coated	Diclofenac potassium 50 mg/1	TabletOral	VICI Pharmaceuticals, Inc	87528-001	87528-0001-10
Diclofenac Potassiumdiclofenac potassium 25 mg	Diclofenac potassium 25 mg/1	Capsule, Liquid filledOral	PureTek Corporation	59088-131	59088-0131-73
Diclofenac Potassium	Diclofenac potassium 50 mg/1	Powder, For solutionOral	Umedica Laboratories USA Inc.	60290-061	60290-0061-0160290-0061-02
Diclofenac Potassium	Diclofenac potassium 50 mg/1	Powder, For solutionOral	Nivagen Pharmaceuticals, Inc.	75834-338	75834-0338-0175834-0338-02
Diclofenac Potassiumdiclofenac potassium tablets	Diclofenac potassium 25 mg/1	Tablet, Film coatedOral	NIVAGEN PHARMACEUTICALS, INC.	75834-337	75834-0337-3075834-0337-60
Diclofenac Potassiumdiclofenac potassium, film coated	Diclofenac potassium 25 mg/1	TabletOral	Happy Robin, LLC	87127-802	87127-0802-60
Diclofenac Potassium	Diclofenac potassium 25 mg/1	Capsule, Liquid filledOral	Lifsa Drugs LLC	72336-432	72336-0432-12
Diclofenac Potassium	Diclofenac potassium 50 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-8411	68788-8411-0168788-8411-0368788-8411-06+1 more

All 68 Diclofenac Potassium NDCs

Other NDCs under ANDA 215787

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

FDA NDC Directory listings under ANDA 215787
Product	Strength	Form · route	Labeler	Product NDC
Diclofenac Potassiumdiclofenac potassium, film coated	Diclofenac potassium 25 mg/1	TabletOral	Cintex Services, LLC	24470-924
Diclofenac Potassiumdiclofenac potassium, film coated	Diclofenac potassium 50 mg/1	TabletOral	Golden State Medical Supply, Inc.	51407-912
Diclofenac Potassiumdiclofenac potassium, film coated	Diclofenac potassium 50 mg/1	TabletOral	Amici Pharma, Inc	69292-552
Diclofenac Potassium	Diclofenac potassium 50 mg/1	Tablet, Film coatedOral	Doc Rx	69306-750
Diclofenac Potassium	Diclofenac potassium 50 mg/1	Tablet, Film coatedOral	SOLA Pharmaceuticals, LLC	70512-750
Diclofenac Potassium	Diclofenac potassium 50 mg/1	Tablet, Film coatedOral	SOLA Pharmaceuticals, LLC	70512-900
Diclofenac Potassiumdiclofenac potassium, film coated	Diclofenac potassium 50 mg/1	TabletOral	Havix Group Inc d-b-a Aavis Pharmaceuticals	71337-046
Diclofenac Potassiumdiclofenac potassium, film coated	Diclofenac potassium 25 mg/1	TabletOral	INA Pharmaceutics Inc,	74157-016
Diclofenac Potassium	Diclofenac potassium 50 mg/1	Tablet, Film coatedOral	Advanced Rx of Tennessee, LLC	80425-0456
Diclofenac Potassium	Diclofenac potassium 50 mg/1	Tablet, Film coatedOral	Advanced Rx of Tennessee, LLC	80425-0457
Diclofenac Potassium	Diclofenac potassium 50 mg/1	Tablet, Film coatedOral	PHOENIX RX LLC	85509-1900
Diclofenac Potassiumdiclofenac potassium, film coated	Diclofenac potassium 25 mg/1	TabletOral	Happy Robin, LLC	87127-802
Diclofenac Potassiumdiclofenac potassium, film coated	Diclofenac potassium 50 mg/1	TabletOral	VICI Pharmaceuticals, Inc	87528-001
Diclofenac Potassiumdiclofenac potassium, film coated	Diclofenac potassium 50 mg/1	TabletOral	Amerisyn LLC	87564-011