All Day Relief is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Rugby Laboratories. The primary component is Naproxen Sodium.
| Product ID | 0536-1022_8b0b968a-70e3-4f6d-af0e-6e78345d4545 |
| NDC | 0536-1022 |
| Product Type | Human Otc Drug |
| Proprietary Name | All Day Relief |
| Generic Name | Naproxen Sodium, Coated Tablets |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2014-03-10 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA090545 |
| Labeler Name | Rugby Laboratories |
| Substance Name | NAPROXEN SODIUM |
| Active Ingredient Strength | 220 mg/1 |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |
| Marketing Start Date | 2014-03-10 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA090545 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2014-03-10 |
| Marketing End Date | 2018-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA090545 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2014-03-10 |
| Marketing End Date | 2018-11-30 |
| Ingredient | Strength |
|---|---|
| NAPROXEN SODIUM | 220 mg/1 |
| SPL SET ID: | 05cf0ab1-293c-4740-84b8-9a4a1cc3e9d9 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0536-1022 | All Day Relief | Naproxen Sodium, Coated Tablets |
| 0536-1023 | All Day Relief | Naproxen Sodium Tablet, coated |
| 42507-140 | all day relief | Naproxen sodium |
| 42507-368 | all day relief | Naproxen Sodium |
| 52959-469 | all day relief | Naproxen Sodium |
| 56062-368 | All Day Relief | Naproxen Sodium |
| 56062-490 | all day relief | Naproxen Sodium |
| 56062-748 | All Day Relief | Naproxen Sodium |
| 68788-9971 | All Day Relief | Naproxen Sodium Tablet, coated |
| 25000-141 | Naproxen Sodium | Naproxen Sodium, Coated Tablets |