Prescription drug · ANDA
Diclofenac Sodium Delayed Release NDC 68071-3184
diclofenac sodium · Diclofenac sodium 50 mg/1 · Tablet, Delayed release · Oral · NuCare Pharmaceuticals, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 68071-3184-1 | 68071318401 | 21 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3184-1)Marketed from Mar 21, 2017 | |
| 68071-3184-2 | 68071318402 | 20 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3184-2)Marketed from Mar 21, 2017 | |
| 68071-3184-3 | 68071318403 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3184-3)Marketed from Mar 21, 2017 | |
| 68071-3184-5 | 68071318405 | 45 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3184-5)Marketed from Mar 21, 2017 | |
| 68071-3184-6 | 68071318406 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3184-6)Marketed from Mar 21, 2017 | |
| 68071-3184-9 | 68071318409 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3184-9)Marketed from Mar 21, 2017 |
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 Delayed ReleaseSuffix: Delayed Release
- Generic name (nonproprietary)
- diclofenac sodium
- Active ingredients
- Diclofenac sodium — 50 mg/1
- Dosage form
- Tablet, Delayed release
- Route
- Oral
- Labeler
- NuCare Pharmaceuticals, Inc.
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 075185
- Marketing start
- Listing expires
- Other FDA classes
- Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)Decreased Prostaglandin Production (Physiologic effect)
- Identifiers
- Product ID 68071-3184_1da0c34e-cc8a-9db7-e063-6394a90afe92SPL ID 1da0c34e-cc8a-9db7-e063-6394a90afe92SPL set ID 4b44ac98-225c-1739-e054-00144ff88e88RxCUI 855906UNII QTG126297QUPC 0368071318463
- 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
N468071318401followed by a unit qualifier and the quantityPackage 68071-3184-01. 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
Label details couldn’t be retrieved right now. Open the label on DailyMed.
Other NDCs under ANDA 075185
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 Delayed Releasediclofenac sodium | Diclofenac sodium 50 mg/1 | Tablet, Delayed releaseOral | REMEDYREPACK INC. | 70518-0756 |
| Diclofenac Sodium Delayed Releasediclofenac sodium | Diclofenac sodium 75 mg/1 | Tablet, Delayed releaseOral | Proficient Rx LP | 63187-222 |
| Diclofenac Sodium Delayed Releasediclofenac sodium | Diclofenac sodium 50 mg/1 | Tablet, Delayed releaseOral | Golden State Medical Supply, Inc. | 51407-967 |
| Diclofenac Sodium Delayed Releasediclofenac sodium | Diclofenac sodium 75 mg/1 | Tablet, Delayed releaseOral | Golden State Medical Supply, Inc. | 51407-968 |
| Diclofenac Sodium DRdiclofenac sodium | Diclofenac sodium 75 mg/1 | Tablet, Delayed releaseOral | Advanced Rx Pharmacy of Tennessee, LLC | 80425-0189 |
| Diclofenac Sodium Delayed Releasediclofenac sodium | Diclofenac sodium 50 mg/1 | Tablet, Delayed releaseOral | A-S Medication Solutions | 50090-0542 |
| Diclofenac Sodium DRdiclofenac sodium | Diclofenac sodium 50 mg/1 | Tablet, Delayed releaseOral | Advanced Rx Pharmacy of Tennessee, LLC | 80425-0197 |
| Diclofenac Sodium Delayed Releasediclofenac sodium | Diclofenac sodium 50 mg/1 | Tablet, Delayed releaseOral | A-S Medication Solutions | 50090-0543 |
| Diclofenac Sodium Delayed Releasediclofenac sodium | Diclofenac sodium 75 mg/1 | Tablet, Delayed releaseOral | A-S Medication Solutions | 50090-0545 |
| Diclofenac Sodium Delayed Releasediclofenac sodium | Diclofenac sodium 75 mg/1 | Tablet, Delayed releaseOral | Bryant Ranch Prepack | 71335-0357 |
| Diclofenac Sodium Delayed Releasediclofenac sodium | Diclofenac sodium 75 mg/1 | Tablet, Delayed releaseOral | REMEDYREPACK INC. | 70518-0627 |
| Diclofenac Sodium D/R | Diclofenac sodium 50 mg/1 | Tablet, Delayed releaseOral | DirectRx | 72189-675 |
| Diclofenac Sodium Delayed Releasediclofenac sodium | Diclofenac sodium 50 mg/1 | Tablet, Delayed releaseOral | Carlsbad Technology, Inc. | 61442-102 |
| Diclofenac Sodium Delayed Releasediclofenac sodium | Diclofenac sodium 25 mg/1 | Tablet, Delayed releaseOral | Carlsbad Technology, Inc. | 61442-101 |
| Diclofenac Sodium Delayed Releasediclofenac sodium | Diclofenac sodium 75 mg/1 | Tablet, Delayed releaseOral | Carlsbad Technology, Inc. | 61442-103 |
| Diclofenac Sodium | Diclofenac sodium 75 mg/1 | Tablet, Delayed releaseOral | AvKARE | 42291-231 |
| Diclofenac Sodium | Diclofenac sodium 50 mg/1 | Tablet, Delayed releaseOral | AvKARE | 42291-230 |
| Diclofenac Sodium Delayed Releasediclofenac sodium | Diclofenac sodium 75 mg/1 | Tablet, Delayed releaseOral | PHOENIX RX LLC | 85509-1103 |
| Diclofenac Sodium Delayed Releasediclofenac sodium | Diclofenac sodium 50 mg/1 | Tablet, Delayed releaseOral | Carlsbad Technology, Inc. | 61442-226 |
| Diclofenac Sodium Delayed Releasediclofenac sodium | Diclofenac sodium 75 mg/1 | Tablet, Delayed releaseOral | Carlsbad Technology, Inc. | 61442-227 |
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