| 69848-010-10 |
69848-010 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20230301 |
N/A |
ANDA |
ANDA091353 |
Granules USA, Inc. |
NAPROXEN SODIUM |
220 mg/1 |
100 TABLET in 1 BOTTLE (69848-010-10) |
| 37835-594-01 |
37835-594 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20250301 |
N/A |
ANDA |
ANDA091353 |
Bi-Mart |
NAPROXEN SODIUM |
220 mg/1 |
100 TABLET in 1 BOTTLE (37835-594-01) |
| 37835-594-03 |
37835-594 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20250301 |
N/A |
ANDA |
ANDA091353 |
Bi-Mart |
NAPROXEN SODIUM |
220 mg/1 |
300 TABLET in 1 BOTTLE (37835-594-03) |
| 62207-327-47 |
62207-327 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20210716 |
N/A |
ANDA |
ANDA091353 |
Granules India Ltd |
NAPROXEN SODIUM |
220 mg/1 |
500 TABLET in 1 BOTTLE (62207-327-47) |
| 62207-327-49 |
62207-327 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20210716 |
N/A |
ANDA |
ANDA091353 |
Granules India Ltd |
NAPROXEN SODIUM |
220 mg/1 |
1000 TABLET in 1 BOTTLE (62207-327-49) |
| 62207-328-41 |
62207-328 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20210716 |
N/A |
ANDA |
ANDA091353 |
Granules India Ltd |
NAPROXEN SODIUM |
220 mg/1 |
24 TABLET in 1 BOTTLE (62207-328-41) |
| 62207-328-42 |
62207-328 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20210716 |
N/A |
ANDA |
ANDA091353 |
Granules India Ltd |
NAPROXEN SODIUM |
220 mg/1 |
50 TABLET in 1 BOTTLE (62207-328-42) |
| 62207-328-43 |
62207-328 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20210716 |
N/A |
ANDA |
ANDA091353 |
Granules India Ltd |
NAPROXEN SODIUM |
220 mg/1 |
100 TABLET in 1 BOTTLE (62207-328-43) |
| 62207-328-47 |
62207-328 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20210716 |
N/A |
ANDA |
ANDA091353 |
Granules India Ltd |
NAPROXEN SODIUM |
220 mg/1 |
500 TABLET in 1 BOTTLE (62207-328-47) |
| 62207-328-49 |
62207-328 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20210716 |
N/A |
ANDA |
ANDA091353 |
Granules India Ltd |
NAPROXEN SODIUM |
220 mg/1 |
1000 TABLET in 1 BOTTLE (62207-328-49) |
| 82501-1576-1 |
82501-1576 |
HUMAN OTC DRUG |
Pain Relief |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20220530 |
N/A |
ANDA |
ANDA091353 |
Gobrands, Inc |
NAPROXEN SODIUM |
220 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (82501-1576-1) |
| 62207-327-43 |
62207-327 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20210716 |
N/A |
ANDA |
ANDA091353 |
Granules India Ltd |
NAPROXEN SODIUM |
220 mg/1 |
100 TABLET in 1 BOTTLE (62207-327-43) |
| 62207-327-42 |
62207-327 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20210716 |
N/A |
ANDA |
ANDA091353 |
Granules India Ltd |
NAPROXEN SODIUM |
220 mg/1 |
50 TABLET in 1 BOTTLE (62207-327-42) |
| 62207-327-41 |
62207-327 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20210716 |
N/A |
ANDA |
ANDA091353 |
Granules India Ltd |
NAPROXEN SODIUM |
220 mg/1 |
24 TABLET in 1 BOTTLE (62207-327-41) |
| 62207-728-24 |
62207-728 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20180608 |
N/A |
ANDA |
ANDA091353 |
Granules India Ltd |
NAPROXEN SODIUM |
220 mg/1 |
24 TABLET in 1 BOTTLE (62207-728-24) |
| 62207-728-49 |
62207-728 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20180608 |
N/A |
ANDA |
ANDA091353 |
Granules India Ltd |
NAPROXEN SODIUM |
220 mg/1 |
1000 TABLET in 1 BOTTLE (62207-728-49) |
| 62207-729-24 |
62207-729 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20180608 |
N/A |
ANDA |
ANDA091353 |
Granules India Ltd |
NAPROXEN SODIUM |
220 mg/1 |
24 TABLET in 1 BOTTLE (62207-729-24) |
| 62207-729-42 |
62207-729 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20180608 |
N/A |
ANDA |
ANDA091353 |
Granules India Ltd |
NAPROXEN SODIUM |
220 mg/1 |
50 TABLET in 1 BOTTLE (62207-729-42) |
| 62207-729-43 |
62207-729 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20180608 |
N/A |
ANDA |
ANDA091353 |
Granules India Ltd |
NAPROXEN SODIUM |
220 mg/1 |
100 TABLET in 1 BOTTLE (62207-729-43) |
| 62207-729-47 |
62207-729 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20180608 |
N/A |
ANDA |
ANDA091353 |
Granules India Ltd |
NAPROXEN SODIUM |
220 mg/1 |
500 TABLET in 1 BOTTLE (62207-729-47) |