NDC codes

FDA NDC Directory
Product NDC (as listed)72888-073Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72888-0073Add 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
72888-073-0072888007300728880073001000 TABLET, COATED in 1 BOTTLE (72888-073-00)Marketed from Dec 19, 2020
72888-073-017288800730172888007301100 TABLET, COATED in 1 BOTTLE (72888-073-01)Marketed from Dec 19, 2020
72888-073-057288800730572888007305500 TABLET, COATED in 1 BOTTLE (72888-073-05)Marketed from Feb 3, 2022
72888-073-30728880073307288800733030 TABLET, COATED in 1 BOTTLE (72888-073-30)Marketed from Dec 19, 2020

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 — 50 mg/1
Dosage form
Tablet, Coated
Route
Oral
Labeler
Advagen Pharma LtdNDC labeler code 72888
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 075229
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)Decreased Prostaglandin Production (Physiologic effect)
Identifiers
Product ID 72888-073_5bfca526-a004-182e-e063-6394a90a2ffcSPL ID 5bfca526-a004-182e-e063-6394a90a2ffc

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

N472888007300 followed by a unit qualifier and the quantity

Package 72888-0073-00. 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 72888-073

What is NDC 72888-073?
72888-073 is the product NDC for Diclofenac Potassium, Diclofenac potassium 50 mg/1 tablet, coated, listed with the FDA by Advagen Pharma Ltd. 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?
Advagen Pharma Ltd, NDC labeler code 72888. 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 coatedOralPreferred Pharmaceuticals Inc.68788-841168788-8411-0168788-8411-0368788-8411-06+1 more

All 68 Diclofenac Potassium NDCs

Other NDCs under ANDA 075229

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

FDA NDC Directory listings under ANDA 075229
ProductStrengthForm · routeLabelerProduct NDC
Diclofenac PotassiumDiclofenac potassium 50 mg/1Tablet, CoatedOralA-S Medication Solutions50090-5893
Diclofenac PotassiumDiclofenac potassium 50 mg/1Tablet, CoatedOralNorthwind Health Company, LLC51655-230
Diclofenac PotassiumDiclofenac potassium 50 mg/1Tablet, CoatedOralCoupler LLC67046-1522
Diclofenac PotassiumDiclofenac potassium 50 mg/1Tablet, CoatedOralNuCare Pharmaceuticals,Inc.68071-2625
Diclofenac PotassiumDiclofenac potassium 50 mg/1Tablet, CoatedOralBryant Ranch Prepack71335-2052
Diclofenac PotassiumDiclofenac potassium 25 mg/1Tablet, CoatedOralAdvagen Pharma Ltd72888-086
Diclofenac PotassiumDiclofenac potassium 75 mg/1Tablet, CoatedOralAdvagen Pharma Ltd72888-203
Diclofenac PotassiumDiclofenac potassium 25 mg/1Tablet, CoatedOralTrifluent Pharma LLC73352-086
Diclofenac PotassiumDiclofenac potassium 25 mg/1Tablet, CoatedOralINA Pharmaceutics Inc74157-007
Diclofenac PotassiumDiclofenac potassium 50 mg/1Tablet, CoatedOralProficient Rx LP82804-010

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