Naproxen All day relief for pain is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Allegiant Health. The primary component is Naproxen Sodium.
| Product ID | 69168-361_1b97ae91-7304-49f3-a5aa-38973bb61c49 |
| NDC | 69168-361 |
| Product Type | Human Otc Drug |
| Proprietary Name | Naproxen All day relief for pain |
| Generic Name | Naproxen Sodium 220 Mg |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2014-12-23 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA090545 |
| Labeler Name | Allegiant Health |
| Substance Name | NAPROXEN SODIUM |
| Active Ingredient Strength | 220 mg/1 |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
| Marketing Start Date | 2014-12-23 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA090545 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2014-12-23 |
| Marketing Category | ANDA |
| Application Number | ANDA090545 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2014-12-23 |
| Marketing Category | ANDA |
| Application Number | ANDA090545 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2014-12-23 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| NAPROXEN SODIUM | 220 mg/1 |
| SPL SET ID: | 1b97ae91-7304-49f3-a5aa-38973bb61c49 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 69168-361 | Naproxen | Naproxen Sodium 220 mg |
| 69168-362 | Naproxen Caplets | Naproxen Sodium 220 mg |
| 69168-394 | Naproxen Caplets | Naproxen Sodium 220 mg |