NDC codes

FDA NDC Directory
Product NDC (as listed)60290-088Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60290-0088Add 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
60290-088-016029000880130 TABLET, FILM COATED in 1 BOTTLE (60290-088-01)Marketed from Sep 28, 2024
60290-088-0260290008802100 TABLET, FILM COATED in 1 BOTTLE (60290-088-02)Marketed from Sep 28, 2024
60290-088-0360290008803500 TABLET, FILM COATED in 1 BOTTLE (60290-088-03)Marketed from Sep 28, 2024
60290-088-04602900088041000 TABLET, FILM COATED in 1 BOTTLE (60290-088-04)Marketed from Sep 28, 2024
60290-088-056029000880560 TABLET, FILM COATED in 1 BOTTLE (60290-088-05)Marketed from Oct 30, 2025

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 tablets
Active ingredients
Diclofenac potassium — 25 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 215750
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)Decreased Prostaglandin Production (Physiologic effect)
Identifiers
Product ID 60290-088_4ff2886d-ca64-3bf4-e063-6394a90ac3aeSPL ID 4ff2886d-ca64-3bf4-e063-6394a90ac3aeSPL set ID 1fa07fbe-3708-4200-b3ff-a920434896b6RxCUI 855942, 857702UNII L4D5UA6CB4UPC 0360290057017, 0360290088011

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

N460290008801 followed by a unit qualifier and the quantity

Package 60290-0088-01. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Carefully consider the potential benefits and risks of diclofenac potassium immediate-release 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)

Other NDCs under ANDA 215750

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

FDA NDC Directory listings under ANDA 215750
ProductStrengthForm · routeLabelerProduct NDC
Diclofenac Potassiumdiclofenac potassium tabletsDiclofenac potassium 50 mg/1Tablet, Film coatedOralZydus Pharmaceuticals (USA) Inc.70710-1832
Diclofenac Potassiumdiclofenac potassium tabletsDiclofenac potassium 50 mg/1Tablet, Film coatedOralUmedica Laboratories USA Inc.60290-057
Diclofenac Potassiumdiclofenac potassium tabletsDiclofenac potassium 50 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-6768
Diclofenac Potassiumdiclofenac potassium tabletsDiclofenac potassium 25 mg/1Tablet, Film coatedOralNIVAGEN PHARMACEUTICALS, INC.75834-337
Diclofenac Potassiumdiclofenac potassium tabletsDiclofenac potassium 50 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-3451
Diclofenac Potassiumdiclofenac potassium tabletsDiclofenac potassium 50 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-9720

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