NDC codes

FDA NDC Directory
Product NDC (as listed)68788-8411Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68788-8411Add 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 NDC11-digit (billing)PackageCopy
68788-8411-16878884110168788841101100 TABLET, FILM COATED in 1 BOTTLE (68788-8411-1)Marketed from Oct 1, 2025
68788-8411-3687888411036878884110330 TABLET, FILM COATED in 1 BOTTLE (68788-8411-3)Marketed from Apr 30, 2025
68788-8411-6687888411066878884110660 TABLET, FILM COATED in 1 BOTTLE (68788-8411-6)Marketed from Apr 30, 2025
68788-8411-9687888411096878884110990 TABLET, FILM COATED in 1 BOTTLE (68788-8411-9)Marketed from Apr 30, 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
Preferred Pharmaceuticals Inc.NDC labeler code 68788
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 075219
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)Decreased Prostaglandin Production (Physiologic effect)
Identifiers
Product ID 68788-8411_a179516c-5cbf-4739-b021-d369ff6242b5SPL ID a179516c-5cbf-4739-b021-d369ff6242b5

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

N468788841101 followed by a unit qualifier and the quantity

Package 68788-8411-01. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 68788-8411

What is NDC 68788-8411?
68788-8411 is the product NDC for Diclofenac Potassium, Diclofenac potassium 50 mg/1 tablet, film coated, listed with the FDA by Preferred Pharmaceuticals Inc.. 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?
Preferred Pharmaceuticals Inc., NDC labeler code 68788. 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Diclofenac PotassiumDiclofenac potassium 75 mg/1Tablet, CoatedOralAdvagen Pharma Ltd72888-20372888-0203-0072888-0203-0172888-0203-05+1 more
Diclofenac Potassiumdiclofenac potassium, film coatedDiclofenac potassium 50 mg/1TabletOralAmerisyn LLC87564-01187564-0011-10
Diclofenac Potassiumdiclofenac potassium, film coatedDiclofenac potassium 50 mg/1TabletOralVICI Pharmaceuticals, Inc87528-00187528-0001-10
Diclofenac Potassiumdiclofenac potassium 25 mgDiclofenac potassium 25 mg/1Capsule, Liquid filledOralPureTek Corporation59088-13159088-0131-73
Diclofenac PotassiumDiclofenac potassium 50 mg/1Powder, For solutionOralUmedica Laboratories USA Inc.60290-06160290-0061-0160290-0061-02
Diclofenac PotassiumDiclofenac potassium 50 mg/1Powder, For solutionOralNivagen Pharmaceuticals, Inc.75834-33875834-0338-0175834-0338-02
Diclofenac Potassiumdiclofenac potassium tabletsDiclofenac potassium 25 mg/1Tablet, Film coatedOralNIVAGEN PHARMACEUTICALS, INC.75834-33775834-0337-3075834-0337-60
Diclofenac Potassiumdiclofenac potassium, film coatedDiclofenac potassium 25 mg/1TabletOralHappy Robin, LLC87127-80287127-0802-60
Diclofenac PotassiumDiclofenac potassium 25 mg/1Capsule, Liquid filledOralLifsa Drugs LLC72336-43272336-0432-12
Diclofenac PotassiumDiclofenac potassium 50 mg/1Tablet, Film coatedOralMarlex Pharmaceuticals, Inc.10135-80610135-0806-01

All 68 Diclofenac Potassium NDCs

Other NDCs under ANDA 075219

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

FDA NDC Directory listings under ANDA 075219
ProductStrengthForm · routeLabelerProduct NDC
Diclofenac PotassiumDiclofenac potassium 50 mg/1Tablet, Film coatedOralTeva Pharmaceuticals USA, Inc.0093-0948
Diclofenac PotassiumDiclofenac potassium 50 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.43063-848
Diclofenac PotassiumDiclofenac potassium 50 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-4108
Diclofenac PotassiumDiclofenac potassium 50 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals, Inc.66267-070

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