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) |
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) |
62207-728-42 |
62207-728 |
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 (62207-728-42) |
62207-728-43 |
62207-728 |
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 (62207-728-43) |
62207-728-47 |
62207-728 |
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 (62207-728-47) |
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) |
62207-761-42 |
62207-761 |
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 (62207-761-42) |
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) |
62207-729-49 |
62207-729 |
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 (62207-729-49) |
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) |
62207-761-43 |
62207-761 |
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 (62207-761-43) |
62207-761-47 |
62207-761 |
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 (62207-761-47) |
62207-761-49 |
62207-761 |
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 (62207-761-49) |
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) |
62207-328-41 |
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) |