RELAFEN DS is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Carwin Pharmaceutical Associates, Llc. The primary component is Nabumetone.
| Product ID | 15370-170_00f18a4b-1509-41fb-8e01-12bfb58f9cca |
| NDC | 15370-170 |
| Product Type | Human Prescription Drug |
| Proprietary Name | RELAFEN DS |
| Generic Name | Nabumetone |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2019-09-20 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA203166 |
| Labeler Name | Carwin Pharmaceutical Associates, LLC |
| Substance Name | NABUMETONE |
| Active Ingredient Strength | 1000 mg/1 |
| Pharm Classes | Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2022-05-12 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA203166 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2020-02-28 |
| Marketing Category | ANDA |
| Application Number | ANDA203166 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2020-02-28 |
| Marketing Category | ANDA |
| Application Number | ANDA203166 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2019-09-20 |
| Ingredient | Strength |
|---|---|
| NABUMETONE | 1000 mg/1 |
| SPL SET ID: | a9a0af85-6c43-4a2d-ba75-0be4ca64c931 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| PHarm Class EPC | |
| UPC Code | |
| NUI Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 15370-170 | RELAFEN DS | NABUMETONE |
| 0115-1657 | Nabumetone | Nabumetone |
| 0115-1658 | Nabumetone | Nabumetone |
| 0440-5843 | Nabumetone | Nabumetone |
| 0440-5844 | Nabumetone | Nabumetone |
| 0591-3670 | Nabumetone | Nabumetone |
| 0591-3671 | Nabumetone | Nabumetone |
| 0615-7630 | Nabumetone | nabumetone |
| 0615-7645 | Nabumetone | nabumetone |
| 0615-7666 | Nabumetone | Nabumetone |
| 0615-7667 | Nabumetone | Nabumetone |
| 10544-003 | Nabumetone | Nabumetone |
| 10544-120 | Nabumetone | Nabumetone |
| 10544-271 | Nabumetone | Nabumetone |
| 10544-273 | Nabumetone | Nabumetone |
| 21695-230 | Nabumetone | Nabumetone |
| 21695-231 | Nabumetone | Nabumetone |
| 33261-077 | Nabumetone | Nabumetone |
| 33261-078 | Nabumetone | Nabumetone |
| 33358-251 | Nabumetone | Nabumetone |
| 33358-252 | Nabumetone | Nabumetone |
| 35356-686 | Nabumetone | Nabumetone |
| 35356-687 | Nabumetone | Nabumetone |
| 35356-726 | Nabumetone | Nabumetone |
| 43063-859 | Nabumetone | Nabumetone |
| 0722-7078 | Nabumetone 1000 mg | Nabumetone |
| 0722-7076 | Nabumetone 500 mg | Nabumetone |
| 0722-7077 | Nabumetone 750 mg | Nabumetone |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() RELAFEN DS 87333917 5944501 Live/Registered |
Argent Development Group, LLC 2017-02-13 |