| 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) |
| 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) |
| 62207-327-41 |
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) |
| 62207-327-42 |
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) |
| 62207-327-43 |
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) |
| 62207-327-47 |
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) |
| 85786-104-24 |
85786-104 |
HUMAN OTC DRUG |
Dr Simi All Day Pain Relief |
Naproxen sodium |
TABLET, FILM COATED |
ORAL |
20250818 |
N/A |
ANDA |
ANDA091353 |
Farmacias De Similares TX LLC |
NAPROXEN SODIUM |
220 mg/1 |
24 TABLET, FILM COATED in 1 BOTTLE (85786-104-24) |
| 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) |
| 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) |
| 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 |
| 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) |
| 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) |