Prescription drug · NDA AUTHORIZED GENERIC
Diclofenac Potassium NDC 71335-2550
Diclofenac potassium 25 mg/1 · Capsule, Liquid filled · Oral · Bryant Ranch Prepack
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71335-2550-1 | 7133525500171335255001 | 30 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
- Labeler
- Bryant Ranch PrepackNDC labeler code 71335
- 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
- Pharmacologic class
- Nonsteroidal Anti-inflammatory Drug
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
N471335255001followed by a unit qualifier and the quantityPackage 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.
About NDC 71335-2550
- What is NDC 71335-2550?
- 71335-2550 is the product NDC for Diclofenac Potassium, Diclofenac potassium 25 mg/1 capsule, liquid filled, listed with the FDA by Bryant Ranch Prepack. It has 1 package NDC, 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?
- Bryant Ranch Prepack, NDC labeler code 71335. 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.
Related NDCs: other Diclofenac Potassium products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Diclofenac Potassium | Diclofenac potassium 75 mg/1 | Tablet, CoatedOral | Advagen Pharma Ltd | 72888-203 | 72888-0203-0072888-0203-0172888-0203-05+1 more |
| Diclofenac Potassiumdiclofenac potassium, film coated | Diclofenac potassium 50 mg/1 | TabletOral | Amerisyn LLC | 87564-011 | 87564-0011-10 |
| Diclofenac Potassiumdiclofenac potassium, film coated | Diclofenac potassium 50 mg/1 | TabletOral | VICI Pharmaceuticals, Inc | 87528-001 | 87528-0001-10 |
| Diclofenac Potassiumdiclofenac potassium 25 mg | Diclofenac potassium 25 mg/1 | Capsule, Liquid filledOral | PureTek Corporation | 59088-131 | 59088-0131-73 |
| Diclofenac Potassium | Diclofenac potassium 50 mg/1 | Powder, For solutionOral | Umedica Laboratories USA Inc. | 60290-061 | 60290-0061-0160290-0061-02 |
| Diclofenac Potassium | Diclofenac potassium 50 mg/1 | Powder, For solutionOral | Nivagen Pharmaceuticals, Inc. | 75834-338 | 75834-0338-0175834-0338-02 |
| Diclofenac Potassiumdiclofenac potassium tablets | Diclofenac potassium 25 mg/1 | Tablet, Film coatedOral | NIVAGEN PHARMACEUTICALS, INC. | 75834-337 | 75834-0337-3075834-0337-60 |
| Diclofenac Potassiumdiclofenac potassium, film coated | Diclofenac potassium 25 mg/1 | TabletOral | Happy Robin, LLC | 87127-802 | 87127-0802-60 |
| Diclofenac Potassium | Diclofenac potassium 25 mg/1 | Capsule, Liquid filledOral | Lifsa Drugs LLC | 72336-432 | 72336-0432-12 |
| Diclofenac Potassium | Diclofenac potassium 50 mg/1 | Tablet, Film coatedOral | Preferred Pharmaceuticals Inc. | 68788-8411 | 68788-8411-0168788-8411-0368788-8411-06+1 more |
Other NDCs under NDA 022202
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Diclofenac Potassium | Diclofenac potassium 25 mg/1 | Capsule, Liquid filledOral | Leading Pharma, LLC | 69315-275 |
| Zipsordiclofenac potassium | Diclofenac potassium 25 mg/1 | Capsule, Liquid filledOral | Assertio Therapeutics, Inc. | 13913-008 |
| Zipsordiclofenac potassium | Diclofenac potassium 25 mg/1 | Capsule, Liquid filledOral | Assertio Specialty Pharmaceuticals LLC | 82497-008 |