69517-109-02 |
69517-109 |
HUMAN OTC DRUG |
All Day Pain Relief |
Naproxen Sodium Tablets, 220 mg |
TABLET |
ORAL |
20160407 |
N/A |
ANDA |
ANDA091353 |
HealthLife of USA LLC |
NAPROXEN SODIUM |
220 mg/1 |
2 POUCH in 1 POUCH (69517-109-02) / 2 TABLET in 1 POUCH |
69517-109-04 |
69517-109 |
HUMAN OTC DRUG |
All Day Pain Relief |
Naproxen Sodium Tablets, 220 mg |
TABLET |
ORAL |
20160407 |
N/A |
ANDA |
ANDA091353 |
HealthLife of USA LLC |
NAPROXEN SODIUM |
220 mg/1 |
400 BOTTLE in 1 BOTTLE (69517-109-04) / 100 BOTTLE in 1 BOTTLE (69517-109-01) / 24 CARTON in 1 BOTTLE (69517-109-24) / 1 TABLET in 1 CARTON |
69517-109-25 |
69517-109 |
HUMAN OTC DRUG |
All Day Pain Relief |
Naproxen Sodium Tablets, 220 mg |
TABLET |
ORAL |
20160407 |
N/A |
ANDA |
ANDA091353 |
HealthLife of USA LLC |
NAPROXEN SODIUM |
220 mg/1 |
25 POUCH in 1 BOX (69517-109-25) / 2 TABLET in 1 POUCH |
69517-109-50 |
69517-109 |
HUMAN OTC DRUG |
All Day Pain Relief |
Naproxen Sodium Tablets, 220 mg |
TABLET |
ORAL |
20160407 |
N/A |
ANDA |
ANDA091353 |
HealthLife of USA LLC |
NAPROXEN SODIUM |
220 mg/1 |
50 POUCH in 1 BOX (69517-109-50) / 2 TABLET in 1 POUCH |
62207-753-47 |
62207-753 |
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 (62207-753-47) |
62207-753-49 |
62207-753 |
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 (62207-753-49) |
62207-753-51 |
62207-753 |
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 (62207-753-51) |
62207-753-52 |
62207-753 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20110930 |
N/A |
ANDA |
ANDA091353 |
Granules India Limited |
NAPROXEN SODIUM |
220 mg/1 |
300 TABLET in 1 BOTTLE (62207-753-52) |
62207-753-53 |
62207-753 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20110930 |
N/A |
ANDA |
ANDA091353 |
Granules India Limited |
NAPROXEN SODIUM |
220 mg/1 |
400 TABLET in 1 BOTTLE (62207-753-53) |
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) |
69848-010-01 |
69848-010 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20190701 |
N/A |
ANDA |
ANDA091353 |
Granules USA, Inc. |
NAPROXEN SODIUM |
220 mg/1 |
10 TABLET in 1 BOTTLE (69848-010-01) |
69848-010-05 |
69848-010 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20230301 |
N/A |
ANDA |
ANDA091353 |
Granules USA, Inc. |
NAPROXEN SODIUM |
220 mg/1 |
50 TABLET in 1 BOTTLE (69848-010-05) |
69848-010-10 |
69848-010 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET |
ORAL |
20230301 |
N/A |
ANDA |
ANDA091353 |
Granules USA, Inc. |
NAPROXEN SODIUM |
220 mg/1 |
100 TABLET in 1 BOTTLE (69848-010-10) |
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) |