| 11822-6040-9 |
11822-6040 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20220718 |
N/A |
ANDA |
ANDA204872 |
Rite Aid Corporation |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (11822-6040-9) / 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
| 11822-6040-6 |
11822-6040 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20220718 |
N/A |
ANDA |
ANDA204872 |
Rite Aid Corporation |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (11822-6040-6) / 200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
| 11822-6040-7 |
11822-6040 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20220718 |
N/A |
ANDA |
ANDA204872 |
Rite Aid Corporation |
NAPROXEN SODIUM |
220 mg/1 |
270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (11822-6040-7) |
| 11822-6040-8 |
11822-6040 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20220718 |
N/A |
ANDA |
ANDA204872 |
Rite Aid Corporation |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (11822-6040-8) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
| 11822-6040-5 |
11822-6040 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20220718 |
N/A |
ANDA |
ANDA204872 |
Rite Aid Corporation |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (11822-6040-5) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
| 27854-170-01 |
27854-170 |
HUMAN OTC DRUG |
AnaDent |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20170123 |
N/A |
ANDA |
ANDA204872 |
Belmora LLC |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (27854-170-01) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
| 71205-595-24 |
71205-595 |
HUMAN OTC DRUG |
Naproxen |
Naproxen Sodium |
TABLET |
ORAL |
20230728 |
N/A |
ANDA |
ANDA204872 |
Proficient Rx LP |
NAPROXEN SODIUM |
220 mg/1 |
24 TABLET in 1 BOTTLE (71205-595-24) |
| 71205-595-30 |
71205-595 |
HUMAN OTC DRUG |
Naproxen |
Naproxen Sodium |
TABLET |
ORAL |
20210727 |
N/A |
ANDA |
ANDA204872 |
Proficient Rx LP |
NAPROXEN SODIUM |
220 mg/1 |
30 TABLET in 1 BOTTLE (71205-595-30) |
| 71205-595-60 |
71205-595 |
HUMAN OTC DRUG |
Naproxen |
Naproxen Sodium |
TABLET |
ORAL |
20210727 |
N/A |
ANDA |
ANDA204872 |
Proficient Rx LP |
NAPROXEN SODIUM |
220 mg/1 |
60 TABLET in 1 BOTTLE (71205-595-60) |
| 71205-595-90 |
71205-595 |
HUMAN OTC DRUG |
Naproxen |
Naproxen Sodium |
TABLET |
ORAL |
20210727 |
N/A |
ANDA |
ANDA204872 |
Proficient Rx LP |
NAPROXEN SODIUM |
220 mg/1 |
90 TABLET in 1 BOTTLE (71205-595-90) |
| 51316-817-08 |
51316-817 |
HUMAN OTC DRUG |
Back and Muscle Pain |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20220418 |
N/A |
ANDA |
ANDA204872 |
CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (51316-817-08) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
| 51316-817-52 |
51316-817 |
HUMAN OTC DRUG |
Back and Muscle Pain |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20220418 |
N/A |
ANDA |
ANDA204872 |
CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (51316-817-52) / 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
| 68788-7572-2 |
68788-7572 |
HUMAN OTC DRUG |
Naproxen |
Naproxen Sodium |
TABLET |
ORAL |
20191227 |
N/A |
ANDA |
ANDA204872 |
Preferred Pharmaceuticals, Inc. |
NAPROXEN SODIUM |
220 mg/1 |
20 TABLET in 1 BOTTLE (68788-7572-2) |
| 68788-7572-3 |
68788-7572 |
HUMAN OTC DRUG |
Naproxen |
Naproxen Sodium |
TABLET |
ORAL |
20191227 |
N/A |
ANDA |
ANDA204872 |
Preferred Pharmaceuticals, Inc. |
NAPROXEN SODIUM |
220 mg/1 |
30 TABLET in 1 BOTTLE (68788-7572-3) |
| 68788-7572-4 |
68788-7572 |
HUMAN OTC DRUG |
Naproxen |
Naproxen Sodium |
TABLET |
ORAL |
20191227 |
N/A |
ANDA |
ANDA204872 |
Preferred Pharmaceuticals, Inc. |
NAPROXEN SODIUM |
220 mg/1 |
40 TABLET in 1 BOTTLE (68788-7572-4) |
| 68788-7572-6 |
68788-7572 |
HUMAN OTC DRUG |
Naproxen |
Naproxen Sodium |
TABLET |
ORAL |
20191227 |
N/A |
ANDA |
ANDA204872 |
Preferred Pharmaceuticals, Inc. |
NAPROXEN SODIUM |
220 mg/1 |
60 TABLET in 1 BOTTLE (68788-7572-6) |
| 27854-160-01 |
27854-160 |
HUMAN OTC DRUG |
Flanax |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20180115 |
N/A |
ANDA |
ANDA204872 |
Belmora LLC |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (27854-160-01) / 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
| 27854-160-24 |
27854-160 |
HUMAN OTC DRUG |
Flanax |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20180115 |
N/A |
ANDA |
ANDA204872 |
Belmora LLC |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (27854-160-24) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
| 42961-122-02 |
42961-122 |
HUMAN OTC DRUG |
First Aid Direct All Day Pain Relief |
Naproxen Sodium |
TABLET, COATED |
ORAL |
20230719 |
N/A |
ANDA |
ANDA204872 |
Cintas Corporation |
NAPROXEN SODIUM |
220 mg/1 |
25 PACKET in 1 BOX (42961-122-02) / 1 TABLET, COATED in 1 PACKET (42961-122-01) |
| 55319-406-15 |
55319-406 |
HUMAN OTC DRUG |
Naproxen |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20231215 |
N/A |
ANDA |
ANDA204872 |
Family Dollar Services Inc |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (55319-406-15) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |