| 0536-1093-11 |
0536-1093 |
HUMAN OTC DRUG |
Rugby All Day Relief |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20220318 |
N/A |
ANDA |
ANDA074661 |
Rugby Laboratories |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE in 1 CARTON (0536-1093-11) / 90 TABLET, FILM COATED in 1 BOTTLE |
| 0536-1094-06 |
0536-1094 |
HUMAN OTC DRUG |
rugby all day relief |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20150902 |
N/A |
ANDA |
ANDA074661 |
Rugby Laboratories |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE in 1 CARTON (0536-1094-06) / 50 TABLET, FILM COATED in 1 BOTTLE |
| 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) |
| 0536-1094-11 |
0536-1094 |
HUMAN OTC DRUG |
rugby all day relief |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20220427 |
N/A |
ANDA |
ANDA074661 |
Rugby Laboratories |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE in 1 CARTON (0536-1094-11) / 90 TABLET, FILM COATED in 1 BOTTLE |
| 0536-1093-06 |
0536-1093 |
HUMAN OTC DRUG |
Rugby All Day Relief |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20150915 |
N/A |
ANDA |
ANDA074661 |
Rugby Laboratories |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE in 1 CARTON (0536-1093-06) / 50 TABLET, FILM COATED in 1 BOTTLE |
| 37808-652-62 |
37808-652 |
HUMAN OTC DRUG |
naproxen sodium |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20171114 |
N/A |
ANDA |
ANDA074661 |
H E B |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE in 1 CARTON (37808-652-62) / 24 TABLET, FILM COATED in 1 BOTTLE |
| 37808-652-71 |
37808-652 |
HUMAN OTC DRUG |
naproxen sodium |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20171114 |
N/A |
ANDA |
ANDA074661 |
H E B |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE in 1 CARTON (37808-652-71) / 50 TABLET, FILM COATED in 1 BOTTLE |
| 37808-713-79 |
37808-713 |
HUMAN OTC DRUG |
naproxen sodium |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20171003 |
N/A |
ANDA |
ANDA074661 |
H E B |
NAPROXEN SODIUM |
220 mg/1 |
400 TABLET, FILM COATED in 1 BOTTLE (37808-713-79) |
| 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 |
| 36800-140-82 |
36800-140 |
HUMAN OTC DRUG |
Topcare All Day Pain Relief |
Naproxen sodium |
TABLET, FILM COATED |
ORAL |
20071203 |
N/A |
ANDA |
ANDA074661 |
Topco Associates LLC |
NAPROXEN SODIUM |
220 mg/1 |
200 TABLET, FILM COATED in 1 BOTTLE (36800-140-82) |
| 37808-631-82 |
37808-631 |
HUMAN OTC DRUG |
naproxen sodium |
Naproxen sodium |
TABLET, FILM COATED |
ORAL |
20171114 |
N/A |
ANDA |
ANDA074661 |
H E B |
NAPROXEN SODIUM |
220 mg/1 |
200 TABLET, FILM COATED in 1 BOTTLE (37808-631-82) |
| 43063-909-20 |
43063-909 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20210327 |
N/A |
ANDA |
ANDA074661 |
PD-Rx Pharmaceuticals, Inc. |
NAPROXEN SODIUM |
220 mg/1 |
20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-909-20) |
| 43063-909-30 |
43063-909 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20210327 |
N/A |
ANDA |
ANDA074661 |
PD-Rx Pharmaceuticals, Inc. |
NAPROXEN SODIUM |
220 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-909-30) |
| 50090-0685-1 |
50090-0685 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20181031 |
N/A |
ANDA |
ANDA074661 |
A-S Medication Solutions |
NAPROXEN SODIUM |
220 mg/1 |
10 TABLET, FILM COATED in 1 BOTTLE (50090-0685-1) |
| 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) |
| 41163-511-71 |
41163-511 |
HUMAN OTC DRUG |
equaline naproxen sodium |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20140924 |
N/A |
ANDA |
ANDA074661 |
United Natural Foods, Inc. dba UNFI |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE in 1 CARTON (41163-511-71) / 50 TABLET, FILM COATED in 1 BOTTLE |
| 41163-511-75 |
41163-511 |
HUMAN OTC DRUG |
equaline naproxen sodium |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20220921 |
N/A |
ANDA |
ANDA074661 |
United Natural Foods, Inc. dba UNFI |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE in 1 CARTON (41163-511-75) / 90 TABLET, FILM COATED in 1 BOTTLE |
| 41163-511-62 |
41163-511 |
HUMAN OTC DRUG |
equaline naproxen sodium |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20140924 |
N/A |
ANDA |
ANDA074661 |
United Natural Foods, Inc. dba UNFI |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE in 1 CARTON (41163-511-62) / 24 TABLET, FILM COATED in 1 BOTTLE |
| 55910-729-62 |
55910-729 |
HUMAN OTC DRUG |
dg health naproxen sodium |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20190612 |
N/A |
ANDA |
ANDA074661 |
Dolgencorp Inc |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE in 1 CARTON (55910-729-62) / 24 TABLET, FILM COATED in 1 BOTTLE |