Naproxen Sodium is a Oral Tablet, Coated in the Human Otc Drug category. It is labeled and distributed by Aaa Pharmaceutical, Inc.. The primary component is Naproxen Sodium.
Product ID | 57344-145_5d765fcc-bfa7-4791-b533-b28f73b01f40 |
NDC | 57344-145 |
Product Type | Human Otc Drug |
Proprietary Name | Naproxen Sodium |
Generic Name | Naproxen Sodium |
Dosage Form | Tablet, Coated |
Route of Administration | ORAL |
Marketing Start Date | 2012-12-15 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA079096 |
Labeler Name | AAA Pharmaceutical, Inc. |
Substance Name | NAPROXEN SODIUM |
Active Ingredient Strength | 220 mg/1 |
NDC Exclude Flag | E |
Listing Certified Through | 2018-12-31 |
Marketing Start Date | 2012-04-01 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA079096 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-04-01 |
Marketing End Date | 2019-09-11 |
Marketing Category | ANDA |
Application Number | ANDA079096 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-04-01 |
Marketing Category | ANDA |
Application Number | ANDA079096 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-04-01 |
Marketing Category | ANDA |
Application Number | ANDA079096 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-04-01 |
Marketing End Date | 2019-09-11 |
Marketing Category | ANDA |
Application Number | ANDA079096 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-04-01 |
Marketing End Date | 2019-09-11 |
Marketing Category | ANDA |
Application Number | ANDA079096 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-04-01 |
Marketing End Date | 2019-09-11 |
Marketing Category | ANDA |
Application Number | ANDA079096 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-04-01 |
Marketing End Date | 2019-09-11 |
Marketing Category | ANDA |
Application Number | ANDA079096 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-04-01 |
Marketing End Date | 2019-09-11 |
Marketing Category | ANDA |
Application Number | ANDA079096 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-04-01 |
Marketing End Date | 2019-09-11 |
Marketing Category | ANDA |
Application Number | ANDA079096 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-04-01 |
Marketing End Date | 2019-09-11 |
Ingredient | Strength |
---|---|
NAPROXEN SODIUM | 220 mg/1 |
SPL SET ID: | 5ea3217d-845d-4781-b849-6b00babdc214 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
68016-056 | Naproxen Sodium | Naproxen Sodium |
68016-661 | Naproxen Sodium | Naproxen Sodium |
68016-660 | Naproxen Sodium | Naproxen Sodium |
68071-3054 | Naproxen Sodium | Naproxen Sodium |
68071-3223 | Naproxen Sodium | Naproxen Sodium |
68210-0040 | NAPROXEN SODIUM | NAPROXEN SODIUM |
68210-0400 | NAPROXEN SODIUM | NAPROXEN SODIUM |
68387-545 | Naproxen Sodium | Naproxen Sodium |
68462-179 | Naproxen Sodium | Naproxen Sodium |
68462-178 | Naproxen Sodium | Naproxen Sodium |
68788-6406 | Naproxen Sodium | Naproxen Sodium |
68788-7304 | Naproxen Sodium | Naproxen Sodium |
68788-6934 | Naproxen Sodium | Naproxen Sodium |
68788-7367 | Naproxen Sodium | Naproxen Sodium |
68788-9022 | Naproxen Sodium | Naproxen Sodium |
68998-144 | NAPROXEN SODIUM | NAPROXEN SODIUM |
68998-145 | NAPROXEN SODIUM | NAPROXEN SODIUM |
69168-632 | Naproxen Sodium | Naproxen Sodium |
69230-305 | Naproxen Sodium | Naproxen Sodium |
69452-179 | Naproxen Sodium | Naproxen Sodium |
69469-169 | Naproxen Sodium | Naproxen Sodium |
69842-010 | naproxen sodium | naproxen sodium |
69842-748 | Naproxen Sodium | Naproxen Sodium |
69842-417 | Naproxen Sodium | Naproxen Sodium |
69842-975 | Naproxen Sodium | Naproxen Sodium |
69842-811 | Naproxen Sodium | Naproxen Sodium |
70518-0409 | Naproxen Sodium | Naproxen Sodium |
70518-0178 | Naproxen sodium | Naproxen sodium |
70518-0724 | Naproxen Sodium | Naproxen Sodium |
70518-1172 | Naproxen Sodium | Naproxen Sodium |
71141-116 | NAPROXEN SODIUM | NAPROXEN SODIUM |
71141-008 | Naproxen Sodium | Naproxen Sodium |
71335-0274 | Naproxen Sodium | Naproxen Sodium |
71335-0822 | Naproxen Sodium | Naproxen Sodium |
71335-1061 | Naproxen Sodium | Naproxen Sodium |
10544-275 | Naproxen Sodium | Naproxen Sodium |
10544-128 | Naproxen Sodium | Naproxen Sodium |
10544-063 | Naproxen Sodium | Naproxen Sodium |
10544-276 | Naproxen Sodium | Naproxen Sodium |
11673-175 | Naproxen Sodium | Naproxen Sodium |
11822-0507 | naproxen sodium | naproxen sodium |
11673-748 | Naproxen Sodium | Naproxen Sodium |
11822-0490 | naproxen sodium | naproxen sodium |
11822-0140 | Naproxen Sodium | Naproxen Sodium |
21130-174 | Naproxen Sodium | Naproxen Sodium |
21130-748 | Naproxen Sodium | Naproxen Sodium |
21695-090 | Naproxen Sodium | Naproxen Sodium |
17856-0194 | Naproxen Sodium | Naproxen Sodium |
25000-141 | Naproxen Sodium | Naproxen Sodium |
25000-144 | Naproxen Sodium | Naproxen Sodium |