Aleve Caplets is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Bayer Healthcare Llc.. The primary component is Naproxen Sodium.
| Product ID | 0280-6000_7a40ecb1-7a61-4962-e053-2a91aa0a5170 |
| NDC | 0280-6000 |
| Product Type | Human Otc Drug |
| Proprietary Name | Aleve Caplets |
| Generic Name | Naproxen Sodium |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2014-02-26 |
| Marketing Category | NDA / NDA |
| Application Number | NDA020204 |
| Labeler Name | Bayer HealthCare LLC. |
| Substance Name | NAPROXEN SODIUM |
| Active Ingredient Strength | 220 mg/1 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2014-02-26 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA |
| Application Number | NDA020204 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2014-02-26 |
| Marketing Category | NDA |
| Application Number | NDA020204 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2016-03-18 |
| Marketing Category | NDA |
| Application Number | NDA020204 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2014-02-26 |
| Marketing Category | NDA |
| Application Number | NDA020204 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2014-02-26 |
| Marketing Category | NDA |
| Application Number | NDA020204 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2014-02-26 |
| Marketing Category | NDA |
| Application Number | NDA020204 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2014-03-26 |
| Marketing Category | NDA |
| Application Number | NDA020204 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2014-02-26 |
| Marketing Category | NDA |
| Application Number | NDA020204 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2016-03-18 |
| Marketing Category | NDA |
| Application Number | NDA020204 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2014-02-26 |
| Marketing Category | NDA |
| Application Number | NDA020204 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2014-02-26 |
| Ingredient | Strength |
|---|---|
| NAPROXEN SODIUM | 220 mg/1 |
| SPL SET ID: | a3745850-3e32-4884-b315-161bcb9996ed |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 70262-301 | Aleve Caplets | Aleve Caplets |
| 0280-6000 | Aleve | NAPROXEN SODIUM |
| 0280-6010 | Aleve | NAPROXEN SODIUM |
| 0280-6020 | Aleve | NAPROXEN SODIUM |
| 0280-0041 | Aleve Headache Pain | Naproxen Sodium |
| 0113-7033 | basic care naproxen sodium | Naproxen Sodium |
| 0113-7368 | Basic Care Naproxen Sodium | Naproxen Sodium |
| 0113-7901 | basic care naproxen sodium | Naproxen Sodium |
| 0113-0901 | Good Sense Naproxen Sodium | Naproxen Sodium |
| 0113-1412 | good sense naproxen sodium | naproxen sodium |
| 0113-1773 | good sense naproxen sodium | Naproxen Sodium |
| 0113-4368 | Good Sense Naproxen Sodium | Naproxen Sodium |
| 0280-0270 | Menstridol | NAPROXEN SODIUM |
| 0143-9908 | NAPROXEN | naproxen sodium |
| 0143-9916 | NAPROXEN | naproxen sodium |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ALEVE 87130338 5279528 Live/Registered |
Bayer HealthCare LLC 2016-08-08 |
![]() ALEVE 86018399 4459303 Live/Registered |
Bayer HealthCare LLC 2013-07-24 |
![]() ALEVE 77105868 3287780 Live/Registered |
Bayer HealthCare LLC 2007-02-13 |
![]() ALEVE 75659920 2321672 Dead/Cancelled |
BAYER CONSUMER CARE LLC 1999-03-12 |
![]() ALEVE 75659913 2321671 Dead/Cancelled |
BAYER CONSUMER CARE LLC 1999-03-12 |
![]() ALEVE 75626019 2323878 Dead/Cancelled |
BAYER CONSUMER CARE LLC 1999-01-25 |
![]() ALEVE 75626018 2346840 Dead/Cancelled |
BAYER CONSUMER CARE LLC 1999-01-25 |
![]() ALEVE 75204472 2177899 Dead/Cancelled |
BAYER HEALTHCARE LLC 1996-11-26 |
![]() ALEVE 73746999 not registered Dead/Abandoned |
RICHARDSON-VICKS INC. 1988-08-18 |
![]() ALEVE 73726530 1536042 Live/Registered |
SYNTEX PUERTO RICO, INC. 1988-05-05 |