| 68788-8443-2 |
68788-8443 |
HUMAN OTC DRUG |
Good Sense Naproxen Sodium |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20230510 |
N/A |
ANDA |
ANDA074661 |
Preferred Pharmaceuticals Inc. |
NAPROXEN SODIUM |
220 mg/1 |
20 TABLET, FILM COATED in 1 BOTTLE (68788-8443-2) |
| 68788-8443-3 |
68788-8443 |
HUMAN OTC DRUG |
Good Sense Naproxen Sodium |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20230510 |
N/A |
ANDA |
ANDA074661 |
Preferred Pharmaceuticals Inc. |
NAPROXEN SODIUM |
220 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (68788-8443-3) |
| 68788-8443-4 |
68788-8443 |
HUMAN OTC DRUG |
Good Sense Naproxen Sodium |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20230510 |
N/A |
ANDA |
ANDA074661 |
Preferred Pharmaceuticals Inc. |
NAPROXEN SODIUM |
220 mg/1 |
40 TABLET, FILM COATED in 1 BOTTLE (68788-8443-4) |
| 68788-8443-6 |
68788-8443 |
HUMAN OTC DRUG |
Good Sense Naproxen Sodium |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20230510 |
N/A |
ANDA |
ANDA074661 |
Preferred Pharmaceuticals Inc. |
NAPROXEN SODIUM |
220 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE (68788-8443-6) |
| 41250-313-82 |
41250-313 |
HUMAN OTC DRUG |
naproxen sodium |
Naproxen sodium |
TABLET, FILM COATED |
ORAL |
20040528 |
N/A |
ANDA |
ANDA074661 |
Meijer Distribution Inc |
NAPROXEN SODIUM |
220 mg/1 |
200 TABLET, FILM COATED in 1 BOTTLE (41250-313-82) |
| 63187-596-24 |
63187-596 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20170901 |
N/A |
ANDA |
ANDA074661 |
Proficient Rx LP |
NAPROXEN SODIUM |
220 mg/1 |
24 TABLET, FILM COATED in 1 BOTTLE (63187-596-24) |
| 63187-596-28 |
63187-596 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20170801 |
N/A |
ANDA |
ANDA074661 |
Proficient Rx LP |
NAPROXEN SODIUM |
220 mg/1 |
28 TABLET, FILM COATED in 1 BOTTLE (63187-596-28) |
| 63187-596-30 |
63187-596 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20150803 |
N/A |
ANDA |
ANDA074661 |
Proficient Rx LP |
NAPROXEN SODIUM |
220 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (63187-596-30) |
| 63187-596-60 |
63187-596 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20150803 |
N/A |
ANDA |
ANDA074661 |
Proficient Rx LP |
NAPROXEN SODIUM |
220 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (63187-596-60) |
| 11673-368-71 |
11673-368 |
HUMAN OTC DRUG |
up and up naproxen sodium |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20090714 |
N/A |
ANDA |
ANDA074661 |
Target Corporation |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE in 1 CARTON (11673-368-71) / 50 TABLET, FILM COATED in 1 BOTTLE |
| 36800-368-62 |
36800-368 |
HUMAN OTC DRUG |
TopCare All Day Pain Relief |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
19970722 |
N/A |
ANDA |
ANDA074661 |
Topco Associates LLC |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE in 1 CARTON (36800-368-62) / 24 TABLET, FILM COATED in 1 BOTTLE |
| 36800-368-71 |
36800-368 |
HUMAN OTC DRUG |
TopCare All Day Pain Relief |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
19970114 |
N/A |
ANDA |
ANDA074661 |
Topco Associates LLC |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE in 1 CARTON (36800-368-71) / 50 TABLET, FILM COATED in 1 BOTTLE |
| 36800-368-75 |
36800-368 |
HUMAN OTC DRUG |
TopCare All Day Pain Relief |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20220712 |
N/A |
ANDA |
ANDA074661 |
Topco Associates LLC |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE in 1 CARTON (36800-368-75) / 90 TABLET, FILM COATED in 1 BOTTLE |
| 36800-368-76 |
36800-368 |
HUMAN OTC DRUG |
TopCare All Day Pain Relief |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20070629 |
N/A |
ANDA |
ANDA074661 |
Topco Associates LLC |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE in 1 CARTON (36800-368-76) / 120 TABLET, FILM COATED in 1 BOTTLE |
| 36800-368-82 |
36800-368 |
HUMAN OTC DRUG |
TopCare All Day Pain Relief |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20040127 |
N/A |
ANDA |
ANDA074661 |
Topco Associates LLC |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE in 1 CARTON (36800-368-82) / 200 TABLET, FILM COATED in 1 BOTTLE |
| 41520-702-75 |
41520-702 |
HUMAN OTC DRUG |
CareOne Naproxen Sodium |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20211230 |
N/A |
ANDA |
ANDA074661 |
American Sales Company |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE in 1 CARTON (41520-702-75) / 90 TABLET, FILM COATED in 1 BOTTLE |
| 68391-368-79 |
68391-368 |
HUMAN OTC DRUG |
Berkley and Jensen Naproxen Sodium |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20110415 |
N/A |
ANDA |
ANDA074661 |
BJWC |
NAPROXEN SODIUM |
220 mg/1 |
400 TABLET, FILM COATED in 1 BOTTLE (68391-368-79) |
| 11673-909-75 |
11673-909 |
HUMAN OTC DRUG |
up and up naproxen sodium |
naproxen sodium |
TABLET, FILM COATED |
ORAL |
20220210 |
N/A |
ANDA |
ANDA074661 |
Target Corporation |
NAPROXEN SODIUM |
220 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (11673-909-75) |
| 50090-3356-0 |
50090-3356 |
HUMAN OTC DRUG |
rugby all day relief |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20180131 |
N/A |
ANDA |
ANDA074661 |
A-S Medication Solutions |
NAPROXEN SODIUM |
220 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (50090-3356-0) |
| 50090-3356-1 |
50090-3356 |
HUMAN OTC DRUG |
rugby all day relief |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20250313 |
N/A |
ANDA |
ANDA074661 |
A-S Medication Solutions |
NAPROXEN SODIUM |
220 mg/1 |
10 TABLET, FILM COATED in 1 BOTTLE (50090-3356-1) |