NDC codes

FDA NDC Directory
Product NDC (as listed)85766-032Labeler and product segments. Claims need a package NDC.
Product NDC at billing width85766-0032Add 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
85766-032-0185766003201100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (85766-032-01)Marketed from Aug 7, 2025
85766-032-07857660032077 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (85766-032-07)Marketed from Aug 7, 2025
85766-032-148576600321414 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (85766-032-14)Marketed from Aug 7, 2025
85766-032-208576600322020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (85766-032-20)Marketed from Aug 7, 2025
85766-032-308576600323030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (85766-032-30)Marketed from Aug 7, 2025
85766-032-608576600326060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (85766-032-60)Marketed from Aug 7, 2025
85766-032-908576600329090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (85766-032-90)Marketed from Aug 7, 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 sodium
Generic name (nonproprietary)
diclofenac sodium
Active ingredients
Diclofenac sodium — 100 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 216275
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)Decreased Prostaglandin Production (Physiologic effect)
Identifiers
Product ID 85766-032_4a2b79c2-3d4a-4fe7-e063-6394a90a3acbSPL ID 4a2b79c2-3d4a-4fe7-e063-6394a90a3acbSPL set ID 99f1e69e-02cf-49c2-83af-3cccbbea4215RxCUI 855657UNII QTG126297Q

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

N485766003201 followed by a unit qualifier and the quantity

Package 85766-0032-01. 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 sodium extended-release tablets and other treatment options before deciding to use diclofenac sodium extended-release tablets. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see WARNINGS ; Gastrointestinal Bleeding, Ulceration, and Perforation ). Diclofenac sodium extended-release tablets are indicated: 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 216275

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

FDA NDC Directory listings under ANDA 216275
ProductStrengthForm · routeLabelerProduct NDC
Diclofenac sodiumDiclofenac sodium 100 mg/1Tablet, Film coatedOralAdvanced Rx of Tennessee, LLC80425-0414
Diclofenac sodiumDiclofenac sodium 100 mg/1Tablet, Film coatedOralAsclemed USA, Inc.76420-598
Diclofenac sodiumDiclofenac sodium 100 mg/1Tablet, Film coatedOralIngenus Pharmaceuticals, LLC50742-278
Diclofenac sodiumDiclofenac sodium 100 mg/1Tablet, Film coatedOralBluePoint Laboratories68001-612
Diclofenac sodiumDiclofenac sodium 100 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-4044
Diclofenac sodiumDiclofenac sodium 100 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-9665

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