What is NDC 59651-353?

59651-353 is the product NDC for Diclofenac Potassium, Diclofenac potassium 25 mg/1 capsule, liquid filled, listed with the FDA by Aurobindo Pharma Limited. It has 2 package NDCs, shown above in 10- and 11-digit form.

Aurobindo Pharma Limited, NDC labeler code 59651. 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 59651-353

NDC codes

FDA NDC Directory

Product NDC (as listed)59651-353Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59651-0353Add 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	Copy
59651-353-01	5965103530159651035301	100 CAPSULE, LIQUID FILLED in 1 BOTTLE (59651-353-01)Marketed from Mar 14, 2022
59651-353-08	5965103530859651035308	120 CAPSULE, LIQUID FILLED in 1 BOTTLE (59651-353-08)Marketed from Mar 14, 2022

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): Diclofenac Potassium
Generic name (nonproprietary): diclofenac potassium
Active ingredients: Diclofenac potassium — 25 mg/1
Dosage form: Capsule, Liquid filled
Route: Oral
Labeler: Aurobindo Pharma LimitedNDC labeler code 59651
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 213875
Marketing start: Mar 14, 2022
Listing expires: Dec 31, 2026
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)Decreased Prostaglandin Production (Physiologic effect)
Identifiers: Product ID 59651-353_69669299-a982-4891-9374-bfa88823c5f2SPL ID 69669299-a982-4891-9374-bfa88823c5f2SPL set ID 7efdbe23-503a-4f38-a0b6-c003033f0de7RxCUI 858342UNII 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

N459651035301 followed by a unit qualifier and the quantity

Package 59651-0353-01. 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 Dec 7, 2024. This label includes a boxed warning.

Indications (excerpt from the label)

Diclofenac potassium capsules are indicated for relief of mild to moderate acute pain in adult and pediatric patients 12 years of age and older. Diclofenac potassium capsules are a non-steroidal anti-inflammatory drug indicated for relief of mild to moderate acute pain in adult and pediatric patients 12 years of age and older. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 59651-353

What is NDC 59651-353?: 59651-353 is the product NDC for Diclofenac Potassium, Diclofenac potassium 25 mg/1 capsule, liquid filled, listed with the FDA by Aurobindo Pharma Limited. It has 2 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?: Aurobindo Pharma Limited, NDC labeler code 59651. 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