Prescription drug · ANDA
Diclofenac Sodium NDC 50090-7855
Diclofenac sodium 75 mg/1 · Tablet, Delayed release · Oral · A-S Medication Solutions
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 50090-7855-0 | 50090785500 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7855-0)Marketed from Jan 14, 2026 | |
| 50090-7855-1 | 50090785501 | 20 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7855-1)Marketed from Jan 14, 2026 | |
| 50090-7855-2 | 50090785502 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7855-2)Marketed from Jan 14, 2026 | |
| 50090-7855-3 | 50090785503 | 14 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7855-3)Marketed from Jan 14, 2026 | |
| 50090-7855-4 | 50090785504 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7855-4)Marketed from Jan 14, 2026 | |
| 50090-7855-8 | 50090785508 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7855-8)Marketed from Jan 14, 2026 | |
| 50090-7855-9 | 50090785509 | 180 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7855-9)Marketed from Jan 14, 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 Sodium
- Generic name (nonproprietary)
- diclofenac sodium
- Active ingredients
- Diclofenac sodium — 75 mg/1
- Dosage form
- Tablet, Delayed release
- Route
- Oral
- Labeler
- A-S Medication Solutions
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 075281
- Marketing start
- Listing expires
- Other FDA classes
- Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)Decreased Prostaglandin Production (Physiologic effect)
- Identifiers
- Product ID 50090-7855_7cd367ac-9d03-4db9-9c8e-1d8dc26aee35SPL ID 7cd367ac-9d03-4db9-9c8e-1d8dc26aee35SPL set ID 6c57e330-ebbe-4165-84a8-4844b2f0097eRxCUI 855926UNII QTG126297Q
- 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
N450090785500followed by a unit qualifier and the quantityPackage 50090-7855-00. 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 delayed-release tablets and other treatment options before deciding to use diclofenac sodium delayed-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 delayed-release tablets are indicated: for relief of the signs and symptoms of osteoarthritis for relief of the signs and symptoms of rheumatoid arthritis for acute or long-term use in the relief of signs and symptoms of ankylosing spondylitis
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 075281
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 Sodium | Diclofenac sodium 75 mg/1 | Tablet, Delayed releaseOral | A-S Medication Solutions | 50090-7856 |
| Diclofenac Sodium | Diclofenac sodium 50 mg/1 | Tablet, Delayed releaseOral | REMEDYREPACK INC. | 70518-4694 |
| Diclofenac Sodium | Diclofenac sodium 75 mg/1 | Tablet, Delayed releaseOral | Aurobindo Pharma Limited | 59651-843 |
| Diclofenac Sodium | Diclofenac sodium 50 mg/1 | Tablet, Delayed releaseOral | Aurobindo Pharma Limited | 59651-842 |
| Diclofenac Sodium | Diclofenac sodium 50 mg/1 | Tablet, Delayed releaseOral | Northwind Health Company, LLC | 82868-101 |
| Diclofenac Sodium | Diclofenac sodium 75 mg/1 | Tablet, Delayed releaseOral | Northwind Health Company, LLC | 82868-114 |
| Diclofenac Sodium | Diclofenac sodium 50 mg/1 | Tablet, Delayed releaseOral | NuCare Pharmaceuticals, Inc. | 68071-5319 |