| 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) |
| 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) |
| 51316-761-20 |
51316-761 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20240525 |
N/A |
ANDA |
ANDA091353 |
CVS |
NAPROXEN SODIUM |
220 mg/1 |
200 TABLET in 1 BOTTLE (51316-761-20) |
| 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) |
| 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) |
| 62207-761-43 |
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) |
| 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) |
| 11673-764-05 |
11673-764 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20240301 |
N/A |
ANDA |
ANDA091353 |
TARGET CORPORATION |
NAPROXEN SODIUM |
220 mg/1 |
50 TABLET in 1 BOTTLE (11673-764-05) |
| 11673-764-09 |
11673-764 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20240301 |
N/A |
ANDA |
ANDA091353 |
TARGET CORPORATION |
NAPROXEN SODIUM |
220 mg/1 |
90 TABLET in 1 BOTTLE (11673-764-09) |
| 55758-048-02 |
55758-048 |
HUMAN OTC DRUG |
Rapidol Naproxen |
Naproxen sodium |
TABLET, COATED |
ORAL |
20231024 |
N/A |
ANDA |
ANDA091353 |
Pharmadel LLC |
NAPROXEN SODIUM |
220 mg/1 |
2 TABLET, COATED in 1 PACKET (55758-048-02) |
| 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) |
| 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) |