NDC codes

FDA NDC Directory
Product NDC (as listed)71335-2550Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-2550Add 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
71335-2550-17133525500130 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-2550-1)Marketed from Jan 21, 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 — 25 mg/1
Dosage form
Capsule, Liquid filled
Route
Oral
Product type
Prescription drug
Marketing category
NDA authorized genericApplication NDA 022202
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)Decreased Prostaglandin Production (Physiologic effect)
Identifiers
Product ID 71335-2550_464b7132-9a4f-4fcf-9338-38fb2cf0056dSPL ID 464b7132-9a4f-4fcf-9338-38fb2cf0056dSPL set ID 69ab6f91-5770-480c-8bd1-8c1f1f8bfdb5RxCUI 858342UNII L4D5UA6CB4

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

N471335255001 followed by a unit qualifier and the quantity

Package 71335-2550-01. 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)

Diclofenac Potassium is indicated for relief of mild to moderate acute pain in adult and pediatric patients 12 years of age and older. Diclofenac potassium is 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)

Other NDCs under NDA 022202

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

FDA NDC Directory listings under NDA 022202
ProductStrengthForm · routeLabelerProduct NDC
Diclofenac PotassiumDiclofenac potassium 25 mg/1Capsule, Liquid filledOralLeading Pharma, LLC69315-275
Zipsordiclofenac potassiumDiclofenac potassium 25 mg/1Capsule, Liquid filledOralAssertio Therapeutics, Inc.13913-008
Zipsordiclofenac potassiumDiclofenac potassium 25 mg/1Capsule, Liquid filledOralAssertio Specialty Pharmaceuticals LLC82497-008

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