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) |
62207-728-24 |
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) |
62207-761-43 |
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) |
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) |
62207-750-41 |
62207-750 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20110930 |
N/A |
ANDA |
ANDA091353 |
Granules India Limited |
NAPROXEN SODIUM |
220 mg/1 |
24 TABLET in 1 BOTTLE (62207-750-41) |
62207-750-42 |
62207-750 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20110930 |
N/A |
ANDA |
ANDA091353 |
Granules India Limited |
NAPROXEN SODIUM |
220 mg/1 |
50 TABLET in 1 BOTTLE (62207-750-42) |
62207-750-43 |
62207-750 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20110930 |
N/A |
ANDA |
ANDA091353 |
Granules India Limited |
NAPROXEN SODIUM |
220 mg/1 |
43 TABLET in 1 BOTTLE (62207-750-43) |
62207-750-44 |
62207-750 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20110930 |
N/A |
ANDA |
ANDA091353 |
Granules India Limited |
NAPROXEN SODIUM |
220 mg/1 |
150 TABLET in 1 BOTTLE (62207-750-44) |
62207-750-45 |
62207-750 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20110930 |
N/A |
ANDA |
ANDA091353 |
Granules India Limited |
NAPROXEN SODIUM |
220 mg/1 |
200 TABLET in 1 BOTTLE (62207-750-45) |
62207-750-47 |
62207-750 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20110930 |
N/A |
ANDA |
ANDA091353 |
Granules India Limited |
NAPROXEN SODIUM |
220 mg/1 |
500 TABLET in 1 BOTTLE (62207-750-47) |
62207-750-49 |
62207-750 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20110930 |
N/A |
ANDA |
ANDA091353 |
Granules India Limited |
NAPROXEN SODIUM |
220 mg/1 |
1000 TABLET in 1 BOTTLE (62207-750-49) |
62207-750-51 |
62207-750 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20110930 |
N/A |
ANDA |
ANDA091353 |
Granules India Limited |
NAPROXEN SODIUM |
220 mg/1 |
10 TABLET in 1 BOTTLE (62207-750-51) |
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 |
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 |