Prescription drug · ANDA
Diclofenac Potassium (Diclofenac potassium tablets) NDC 71335-9720
Diclofenac potassium 50 mg/1 · Tablet, Film coated · Oral · Bryant Ranch Prepack
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71335-9720-1 | 7133597200171335972001 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-9720-1)Marketed from Apr 9, 2026 | |
| 71335-9720-2 | 7133597200271335972002 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-9720-2)Marketed from Oct 17, 2023 | |
| 71335-9720-3 | 7133597200371335972003 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-9720-3)Marketed from May 11, 2023 | |
| 71335-9720-4 | 7133597200471335972004 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-9720-4)Marketed from Nov 15, 2023 | |
| 71335-9720-5 | 7133597200571335972005 | 45 TABLET, FILM COATED in 1 BOTTLE (71335-9720-5)Marketed from Apr 9, 2026 | |
| 71335-9720-6 | 7133597200671335972006 | 58 TABLET, FILM COATED in 1 BOTTLE (71335-9720-6)Marketed from Apr 9, 2026 | |
| 71335-9720-7 | 7133597200771335972007 | 18 TABLET, FILM COATED in 1 BOTTLE (71335-9720-7)Marketed from Apr 9, 2026 | |
| 71335-9720-8 | 7133597200871335972008 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-9720-8)Marketed from Apr 9, 2026 | |
| 71335-9720-9 | 7133597200971335972009 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-9720-9)Marketed from Apr 9, 2026 |
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 tablets
- Active ingredients
- Diclofenac potassium — 50 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Bryant Ranch PrepackNDC labeler code 71335
- 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 71335-9720_78a4857d-93b6-4a0e-93fc-75b02be9fa61SPL ID 78a4857d-93b6-4a0e-93fc-75b02be9fa61SPL set ID 94898228-c595-4fd6-acc2-13dbdbde9c0eRxCUI 855942UNII 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
N471335972001followed by a unit qualifier and the quantityPackage 71335-9720-01. 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.
About NDC 71335-9720
- What is NDC 71335-9720?
- 71335-9720 is the product NDC for Diclofenac Potassium (diclofenac potassium tablets), Diclofenac potassium 50 mg/1 tablet, film coated, listed with the FDA by Bryant Ranch Prepack. It has 9 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Diclofenac Potassium (Diclofenac Potassium Tablets).
- 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 ANDA 215750
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 Potassiumdiclofenac potassium tablets | Diclofenac potassium 50 mg/1 | Tablet, Film coatedOral | A-S Medication Solutions | 50090-6768 |
| Diclofenac Potassiumdiclofenac potassium tablets | Diclofenac potassium 50 mg/1 | Tablet, Film coatedOral | Umedica Laboratories USA Inc. | 60290-057 |
| Diclofenac Potassiumdiclofenac potassium tablets | Diclofenac potassium 25 mg/1 | Tablet, Film coatedOral | Umedica Laboratories USA Inc. | 60290-088 |
| Diclofenac Potassiumdiclofenac potassium tablets | Diclofenac potassium 50 mg/1 | Tablet, Film coatedOral | NuCare Pharmaceuticals,Inc. | 68071-3451 |
| Diclofenac Potassiumdiclofenac potassium tablets | Diclofenac potassium 50 mg/1 | Tablet, Film coatedOral | Zydus Pharmaceuticals (USA) Inc. | 70710-1832 |
| Diclofenac Potassiumdiclofenac potassium tablets | Diclofenac potassium 25 mg/1 | Tablet, Film coatedOral | NIVAGEN PHARMACEUTICALS, INC. | 75834-337 |