| 55758-048-24 |
55758-048 |
HUMAN OTC DRUG |
Rapidol Naproxen |
Naproxen sodium |
TABLET, COATED |
ORAL |
20191009 |
N/A |
ANDA |
ANDA091353 |
Pharmadel LLC |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE in 1 CARTON (55758-048-24) / 24 TABLET, COATED in 1 BOTTLE |
| 55758-048-50 |
55758-048 |
HUMAN OTC DRUG |
Rapidol Naproxen |
Naproxen sodium |
TABLET, COATED |
ORAL |
20231024 |
N/A |
ANDA |
ANDA091353 |
Pharmadel LLC |
NAPROXEN SODIUM |
220 mg/1 |
25 PACKET in 1 CARTON (55758-048-50) / 2 TABLET, COATED in 1 PACKET (55758-048-02) |
| 21130-062-05 |
21130-062 |
HUMAN OTC DRUG |
Naproxen |
Naproxen |
TABLET |
ORAL |
20230830 |
N/A |
ANDA |
ANDA091353 |
Safeway, Inc |
NAPROXEN SODIUM |
220 mg/1 |
50 TABLET in 1 BOTTLE (21130-062-05) |
| 21130-062-09 |
21130-062 |
HUMAN OTC DRUG |
Naproxen |
Naproxen |
TABLET |
ORAL |
20230830 |
N/A |
ANDA |
ANDA091353 |
Safeway, Inc |
NAPROXEN SODIUM |
220 mg/1 |
90 TABLET in 1 BOTTLE (21130-062-09) |
| 21130-062-20 |
21130-062 |
HUMAN OTC DRUG |
Naproxen |
Naproxen |
TABLET |
ORAL |
20230930 |
N/A |
ANDA |
ANDA091353 |
Safeway, Inc |
NAPROXEN SODIUM |
220 mg/1 |
200 TABLET in 1 BOTTLE (21130-062-20) |
| 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) |
| 51316-762-70 |
51316-762 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20240525 |
N/A |
ANDA |
ANDA091353 |
CVS |
NAPROXEN SODIUM |
220 mg/1 |
270 TABLET in 1 BOTTLE (51316-762-70) |
| 69729-123-24 |
69729-123 |
HUMAN OTC DRUG |
PROXEN NP 660 |
Naproxen Sodium |
TABLET |
ORAL |
20231116 |
N/A |
ANDA |
ANDA091353 |
OPMX LLC |
NAPROXEN SODIUM |
220 mg/1 |
2 BLISTER PACK in 1 CARTON (69729-123-24) / 12 TABLET in 1 BLISTER PACK |
| 69729-123-50 |
69729-123 |
HUMAN OTC DRUG |
PROXEN NP 660 |
Naproxen Sodium |
TABLET |
ORAL |
20231107 |
N/A |
ANDA |
ANDA091353 |
OPMX LLC |
NAPROXEN SODIUM |
220 mg/1 |
50 POUCH in 1 CARTON (69729-123-50) / 2 TABLET in 1 POUCH |
| 69729-123-12 |
69729-123 |
HUMAN OTC DRUG |
PROXEN NP 660 |
Naproxen Sodium |
TABLET |
ORAL |
20231107 |
N/A |
ANDA |
ANDA091353 |
OPMX LLC |
NAPROXEN SODIUM |
220 mg/1 |
1 BLISTER PACK in 1 CARTON (69729-123-12) / 12 TABLET in 1 BLISTER PACK |
| 68210-4096-1 |
68210-4096 |
HUMAN OTC DRUG |
NAPROXEN SODIUM |
NAPROXEN SODIUM |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20200702 |
N/A |
ANDA |
ANDA091353 |
SPIRIT PHARMACEUTICALS,LLC |
NAPROXEN SODIUM |
220 mg/1 |
365 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68210-4096-1) |
| 62207-762-42 |
62207-762 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20110930 |
N/A |
ANDA |
ANDA091353 |
Granules India Ltd |
NAPROXEN SODIUM |
220 mg/1 |
50 TABLET, FILM COATED in 1 BOTTLE (62207-762-42) |
| 62207-762-43 |
62207-762 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20110930 |
N/A |
ANDA |
ANDA091353 |
Granules India Ltd |
NAPROXEN SODIUM |
220 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (62207-762-43) |
| 62207-762-47 |
62207-762 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20110930 |
N/A |
ANDA |
ANDA091353 |
Granules India Ltd |
NAPROXEN SODIUM |
220 mg/1 |
500 TABLET, FILM COATED in 1 BOTTLE (62207-762-47) |
| 62207-762-49 |
62207-762 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20110930 |
N/A |
ANDA |
ANDA091353 |
Granules India Ltd |
NAPROXEN SODIUM |
220 mg/1 |
1000 TABLET, FILM COATED in 1 BOTTLE (62207-762-49) |
| 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) |